A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151850



Internal ID15872951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784055..8821239hg38UCSC Ensembl
Innerchr3:8825741..8862925hg19UCSC Ensembl
Innerchr3:8800741..8837925hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3837185
hg1937185
hg1837185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589628
Supporting Variants
SamplesHGDP00084
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151850
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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