A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639535



Internal ID18591130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133946159..134064530hg38UCSC Ensembl
Innerchr4:134867314..134985685hg19UCSC Ensembl
Innerchr4:135086764..135205135hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38118372
hg19118372
hg18118372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023249
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639535
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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