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Human Genome Region 1Q21

Assembly:
GRCh37.p12
Location:
chr1:143,871,003-150,440,213
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-1287 Resolved 1q21 region of the Reference Assembly is composed of multiple haplotypes and gaps The new tilepath has been uploaded to both the Chromosome level TPF for Chromosome 1.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH636052.4 NW_003871055.3 FIX 7,283,150 8,557 2,552,240
           

1Q21 -- chr1 (NC_000001.10):143,871,003-150,440,213