A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525427



Internal ID18823708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86409582..86448695hg38UCSC Ensembl
Innerchr13:87061837..87100950hg19UCSC Ensembl
Innerchr13:85859838..85898951hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3839114
hg1939114
hg1839114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044558
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)nssv3525427
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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