A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585662



Internal ID6625977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32070364..32072051hg38UCSC Ensembl
Innerchr1:32070364..32072051hg38UCSC Ensembl
Outerchr1:32070229..32072258hg38UCSC Ensembl
chr1:32535965..32537652hg19UCSC Ensembl
Innerchr1:32535965..32537652hg19UCSC Ensembl
Outerchr1:32535830..32537859hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381688
hg191688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9896320, essv9896321
SamplesNA19054, NA18946
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585662
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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