A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639534



Internal ID18591129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133927213..133972919hg38UCSC Ensembl
Innerchr4:134848368..134894074hg19UCSC Ensembl
Innerchr4:135067818..135113524hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3845707
hg1945707
hg1845707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032864
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)nssv3639534
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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