A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3629623



Internal ID18581218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68509618..68586170hg38UCSC Ensembl
Innerchr4:69375336..69451888hg19UCSC Ensembl
Innerchr4:69057931..69134483hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3876553
hg1976553
hg1876553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009722
Supporting Variants
Samples
Known GenesUGT2B17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3629623
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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