A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581718



Internal ID16022441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45531122..45532102hg38UCSC Ensembl
Innerchr2:45758261..45759241hg19UCSC Ensembl
Innerchr2:45611765..45612745hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38981
hg19981
hg18981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv908054
Samples
Known GenesSRBD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581718
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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