A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv711663



Internal ID16005619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24568506..24621457hg38UCSC Ensembl
Innerchr1:24894997..24947948hg19UCSC Ensembl
Innerchr1:24767584..24820535hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3852952
hg1952952
hg1852952
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545823
Supporting Variants
Samples
Known GenesNCMAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv711663
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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