A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639487



Internal ID18937768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131587715..131626271hg38UCSC Ensembl
Innerchr4:132508870..132547426hg19UCSC Ensembl
Innerchr4:132728320..132766876hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3838557
hg1938557
hg1838557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016565
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)nssv3639487
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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