A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581405



Internal ID16368814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35593041..35862576hg38UCSC Ensembl
Innerchr2:35818107..36087642hg19UCSC Ensembl
Innerchr2:35671611..35941146hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38269536
hg19269536
hg18269536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6771n54
Supporting Variantsnssv906224
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581405
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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