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Human Genome Region LRC

Assembly:
GRCh37.p13
Location:
chr19:54,528,888-55,595,686
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL949746.1 NW_003571054.1 NOVEL 987,716 1,108 649
GL949747.1 NW_003571055.1 NOVEL 729,519 1,694 28,092
GL949748.1 NW_003571056.1 NOVEL 1,064,303 1,495 12,373
GL949749.1 NW_003571057.1 NOVEL 1,091,840 716 75
GL949750.1 NW_003571058.1 NOVEL 1,066,389 87 23
GL949751.1 NW_003571059.1 NOVEL 1,002,682 453 61
GL949752.1 NW_003571060.1 NOVEL 987,100 1,152 1,232
GL949753.1 NW_003571061.1 NOVEL 796,478 850 17,977
KB021647.1 NW_004166865.1 FIX 1,058,686 1,742 2,168
           

LRC -- chr19 (NC_000019.9):54,528,888-55,595,686