A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016886



Internal ID18759421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:38936517..39002988hg38UCSC Ensembl
Innerchr5:38936619..39003090hg19UCSC Ensembl
Innerchr5:38972376..39038847hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3866472
hg1966472
hg1866472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5636n100
Supporting Variantsnssv3637098
Samples
Known GenesRICTOR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016886
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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