A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581017



Internal ID16368426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14113086..14172737hg38UCSC Ensembl
Innerchr2:14253211..14312862hg19UCSC Ensembl
Innerchr2:14170662..14230313hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3859652
hg1959652
hg1859652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6701n54
Supporting Variantsnssv903820
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581017
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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