A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639431



Internal ID18591026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:127889372..128028165hg38UCSC Ensembl
Innerchr4:128810527..128949320hg19UCSC Ensembl
Innerchr4:129029977..129168770hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38138794
hg19138794
hg18138794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019193
Supporting Variants
Samples
Known GenesC4orf29, 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)nssv3639431
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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