A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513649



Internal ID18465244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79138318..79313758hg38UCSC Ensembl
Innerchr10:80898075..81073515hg19UCSC Ensembl
Innerchr10:80568081..80743521hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38175441
hg19175441
hg18175441
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051195
Supporting Variants
Samples
Known GenesZMIZ1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3513649
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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