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Human Genome Region DGKK_REGION98

Assembly:
GRCh37.p11
Location:
chrX:47,619,971-54,424,077
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-1253 Resolved cDNA AB183864.1 nucleotide 3121 is missing from the reference genome. It is a coding exon of the DGKK gene. The deletion in AL591367 was a a result of a sequencing error. This base has now been corrected in the accession and Genbank has been updated.
HG-1432 Resolved Ampliconic region of Chromosome X (NC_000023.10:48,500,000-49,260,000) consists of multiple haplotypes. This new TPF has been uploaded to the patches TPF and chromosome TPF.
HG-1433 Resolved Ampliconic region of Chromosome X (NC_000023.10:50,025,000-54,060,000) consists of multiple haplotypes. This new TPF has been uploaded to the patches TPF and chromosome TPF.
HG-1436 Resolved An RP11 clone pathway is being sequenced for an ampliconic region on Chromosome X between components Z98304.1 and AF196972.1 of GRCh37. This new TPF has been uploaded to the patches TPF and chromosome TPF.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH806587.1 NW_004070877.1 FIX 4,110,759 591 19,483
JH806590.2 NW_004070880.2 FIX 2,418,393 1,033 30,160
           

DGKK_REGION98 -- chrX (NC_000023.10):47,619,971-54,424,077