A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151068



Internal ID15880169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41001448..41028402hg38UCSC Ensembl
Innerchr2:41228588..41255542hg19UCSC Ensembl
Innerchr2:41082092..41109046hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3826955
hg1926955
hg1826955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581544
Supporting Variants
SamplesNINDS_166
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151068
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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