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Human Genome Region REGION66

Assembly:
GRCh37.p12
Location:
chr19:8,634,915-8,926,179
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-729 Resolved Reference Assembly gap between AC145203.1 and AC130468.2 RP11-468O16 (AC243312.2) has been sequenced to close this gap, making AC130468.2, AC092312.3, AC092566.2 and AC093230.2 redundant.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH159149.1 NW_003871094.1 FIX 245,473 472 6,233
           

REGION66 -- chr19 (NC_000019.9):8,634,915-8,926,179