A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3637986



Internal ID18936267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:46195769..46389159hg38UCSC Ensembl
Innerchr5:46195871..46389261hg19UCSC Ensembl
Innerchr5:46231628..46425018hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38193391
hg19193391
hg18193391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028629
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)nssv3637986
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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