A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997335



Internal ID19156873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68580436..68612596hg38UCSC Ensembl
Innerchr3:68629587..68661747hg19UCSC Ensembl
Innerchr3:68712277..68744437hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3832161
hg1932161
hg1832161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593977, nssv3593976
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)nsv997335
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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