A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151751



Internal ID15875515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21215817..21303734hg38UCSC Ensembl
Innerchr3:21257309..21345226hg19UCSC Ensembl
Innerchr3:21232313..21320230hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3887918
hg1987918
hg1887918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589888
Supporting Variants
SamplesHGDP00695
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151751
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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