A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710254



Internal ID16004210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13986985..14044642hg38UCSC Ensembl
Innerchr1:14313480..14371137hg19UCSC Ensembl
Innerchr1:14186067..14243724hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3857658
hg1957658
hg1857658
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545569
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)nssv710254
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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