A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639695



Internal ID18937976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702410..8746922hg38UCSC Ensembl
Innerchr5:8702522..8747034hg19UCSC Ensembl
Innerchr5:8755522..8800034hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3844513
hg1944513
hg1844513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018839
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)nssv3639695
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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