A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999246



Internal ID19158782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162729460..162908195hg38UCSC Ensembl
Innerchr3:162447248..162625983hg19UCSC Ensembl
Innerchr3:163929942..164108677hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38178736
hg19178736
hg18178736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741572
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999246
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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