A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3529328



Internal ID18827609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70167253..70198262hg38UCSC Ensembl
Innerchr13:70741385..70772394hg19UCSC Ensembl
Innerchr13:69639386..69670395hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3831010
hg1931010
hg1831010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038142
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)nssv3529328
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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