A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710902



Internal ID15658172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16903496..16916236hg38UCSC Ensembl
Innerchr1:17229991..17242731hg19UCSC Ensembl
Innerchr1:17102578..17115318hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3812741
hg1912741
hg1812741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545677
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710902
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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