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Human Genome Region TRB

Assembly:
GRCh37.p13
Location:
chr7:141,557,850-142,778,624
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-7 Resolved ESP analysis suggests the reference chromosome contains an insertion within U66059.1 This ALT_LOCI provides a single library representation of the TRBV region, in contrast to the conglomerates of YACs from mixed libraries that represented this region in GRCh37 NC_000007.13. The reference has been replaced with the single haplotype CH17 Pathway in this region, tracked in HG-1336.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL582971.1 NW_003571040.1 FIX 1,284,284 441 165,197
           

TRB -- chr7 (NC_000007.13):141,557,850-142,778,624