A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3637901



Internal ID18936182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:46000661..46389159hg38UCSC Ensembl
Innerchr5:46000763..46389261hg19UCSC Ensembl
Innerchr5:46036520..46425018hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38388499
hg19388499
hg18388499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025880
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)nssv3637901
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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