A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580926



Internal ID16021649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9405901..9406524hg38UCSC Ensembl
Innerchr2:9546030..9546653hg19UCSC Ensembl
Innerchr2:9463481..9464104hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38624
hg19624
hg18624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6685n54
Supporting Variantsnssv903595
Samples
Known GenesITGB1BP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580926
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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