A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9895563



Internal ID4801145
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585642
Supporting Variants
SamplesNA11933
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9895563
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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