A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585522



Internal ID6625840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25266151..25334731hg38UCSC Ensembl
chr1:25592642..25661222hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3868581
hg1968581
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9893109, essv9893102, essv9893104, essv9893106, essv9893105, essv9893101, essv9893103, essv9893108, essv9893110, essv9893107, essv9893100
SamplesNA19026, HG02979, HG02944, NA12776, HG03756, HG02078, HG00102, NA18646, HG03025, NA19204, HG01462
Known GenesRHD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585522
Frequency
Sample Size2504
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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