A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625054



Internal ID18923335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44361470..44474962hg38UCSC Ensembl
Innerchr4:44363487..44476979hg19UCSC Ensembl
Innerchr4:44058244..44171736hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38113493
hg19113493
hg18113493
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002150
Supporting Variants
Samples
Known GenesKCTD8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3625054
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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