A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638514



Internal ID18936795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2038016..2072758hg38UCSC Ensembl
Innerchr5:2038130..2072872hg19UCSC Ensembl
Innerchr5:2091130..2125872hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3834743
hg1934743
hg1834743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032941
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)nssv3638514
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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