A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173821



Internal ID15853768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:40881556..40908478hg38UCSC Ensembl
Innerchr1:41347228..41374150hg19UCSC Ensembl
Innerchr1:41119815..41146737hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3826923
hg1926923
hg1826923
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546095
Supporting Variants
Samples1780854436_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173821
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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