A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3647003



Internal ID18945284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:108655725..108692522hg38UCSC Ensembl
Innerchr5:107991426..108028223hg19UCSC Ensembl
Innerchr5:108019325..108056122hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3836798
hg1936798
hg1836798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024076
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)nssv3647003
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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