A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719662



Internal ID16013618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:99054986..99086252hg38UCSC Ensembl
Innerchr1:99520542..99551808hg19UCSC Ensembl
Innerchr1:99293130..99324396hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3831267
hg1931267
hg1831267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546885
Supporting Variants
Samples
Known GenesLOC100129620
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv719662
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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