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Human Genome Region REGION49

Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-281 Resolved Comparison to Chimp and Venter suggest missing sequence in reference. AP006622 replaced by FP710250.11 to resolve 63kb deletion in AP006622. Component FP710250.10 corrects a deletion found in GRCh37 chromosome NC_000011.9, in component AP006622.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL582973.1 NW_003571045.1 FIX 321,004 146 62,416

REGION49 -- chr11 (NC_000011.9):49,862,648-50,121,284