A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638200



Internal ID18936481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10837947..10962610hg38UCSC Ensembl
Innerchr5:10838059..10962722hg19UCSC Ensembl
Innerchr5:10891059..11015722hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38124664
hg19124664
hg18124664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027810
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)nssv3638200
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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