A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581736



Internal ID16022459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45531809..45532735hg38UCSC Ensembl
Innerchr2:45758948..45759874hg19UCSC Ensembl
Innerchr2:45612452..45613378hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38927
hg19927
hg18927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6846n54
Supporting Variantsnssv908092
Samples
Known GenesSRBD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581736
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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