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Region information for REGION76

Organism:
Human
Assembly:
GRCh37.p12
Region:
chrX:75,200,416-77,450,502
Cytogenetic location:

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Issue information
JIRA ticket ID Status Description Resolution text
HG-1425 Resolved This issue duplicates a portion of of HG-1381, and has been created solely for the release of a fix patch encompassing the GRCh37 ampliconic sub-region from AC233982.2 to CR407552.3. This patch provides a single haplotype representation for the ampliconic region between GRCh37 NC_000023.10 components AC233982.2 and CR407552.3, in contrast to the mixed haplotype that is present in GRCh37.
HG-1426 Resolved This issue duplicates a portion of of HG-1381, and has been created solely for the release of a fix patch encompassing the GRCh37 ampliconic sub-region from BX682239.3 to AL138743.5 This patch provides a single haplotype representation for the ampliconic region between GRCh37 NC_000023.10 components BX682239 and AL138743, in contrast to the mixed haplotype that is present in GRCh37.
Sequence information
GenBank ID RefSeq ID Sequence Type Length Alignment mismatch Unique sequence Show in Viewer
JH720453.1 NW_003871100.1 Fix 1,461,188 1,171 8,813
JH720454.3 NW_003871101.3 Fix 752,267 98 5,569
           

chrX (NC_000023.10):75,200,416-77,450,502