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Human Genome Region REGION99

Assembly:
GRCh37.p11
Location:
chr6:169,194,170-169,351,741
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-1075 Resolved Possible under-representation of tandem repeat copy number in reference component AL513210.32. AC225168.3 represents a sequence variant containing approximately 30kb more of a tandem repeat sequence than is found in GRCh37 NC_000006.11 component AL513210.32. This has been added to the ALT_REF_LOCI_1 TPF.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KB021644.1 NW_004166862.1 NOVEL 187,824 96 30,274
           

REGION99 -- chr6 (NC_000006.11):169,194,170-169,351,741