A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998698



Internal ID19158234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:31342136..31368538hg38UCSC Ensembl
Innerchr3:31383628..31410030hg19UCSC Ensembl
Innerchr3:31358632..31385034hg18UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3826403
hg1926403
hg1826403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589581
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)nsv998698
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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