A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585642



Internal ID6973162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31102087..31104352hg38UCSC Ensembl
Innerchr1:31102246..31104302hg38UCSC Ensembl
Outerchr1:31102021..31104418hg38UCSC Ensembl
chr1:31574934..31577199hg19UCSC Ensembl
Innerchr1:31575093..31577149hg19UCSC Ensembl
Outerchr1:31574868..31577265hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg382266
hg192266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9895563, essv9895562, essv9895559, essv9895561, essv9895564, essv9895560, essv9895565
SamplesNA11933, HG00367, NA12413, HG01080, NA12878, HG01101, HG00362
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585642
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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