A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033992



Internal ID19123214
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 StatusM
Merged Variantsdgv5798n100
Supporting Variantsnssv3746602
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)nsv1033992
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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