A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004362



Internal ID19093579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119014263..119101798hg38UCSC Ensembl
Innerchr3:118733110..118820645hg19UCSC Ensembl
Innerchr3:120215800..120303335hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3887536
hg1987536
hg1887536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4844n100
Supporting Variantsnssv3604499, nssv3604494, nssv3735278, nssv3735279, nssv3735276, nssv3604500, nssv3604498, nssv3604497, nssv3604495, nssv3604496, nssv3735277
Samples
Known GenesIGSF11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004362
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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