A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638519



Internal ID18936800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2763844..2790207hg38UCSC Ensembl
Innerchr5:2763958..2790321hg19UCSC Ensembl
Innerchr5:2816958..2843321hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3826364
hg1926364
hg1826364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016693
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)nssv3638519
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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