A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746602



Internal ID19044883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120709552..120896460hg38UCSC Ensembl
Innerchr5:120045247..120232155hg19UCSC Ensembl
Innerchr5:120073146..120260054hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38186909
hg19186909
hg18186909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033992
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)nssv3746602
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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