A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648231



Internal ID18946512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:162267897..162445880hg38UCSC Ensembl
Innerchr5:161694903..161872886hg19UCSC Ensembl
Innerchr5:161627481..161805464hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38177984
hg19177984
hg18177984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032616
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)nssv3648231
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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