A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963566



Internal ID16257522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63286358..63287265hg38UCSC Ensembl
Innerchr3:63272034..63272941hg19UCSC Ensembl
Innerchr3:63247074..63247981hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38908
hg19908
hg18908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590452
Supporting Variants
Samples
Known GenesSYNPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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