A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639430



Internal ID18591025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:127882004..128173863hg38UCSC Ensembl
Innerchr4:128803159..129095018hg19UCSC Ensembl
Innerchr4:129022609..129314468hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38291860
hg19291860
hg18291860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033701
Supporting Variants
Samples
Known GenesC4orf29, LARP1B, MFSD8, PLK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639430
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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