A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3529347



Internal ID18827628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70167253..70201627hg38UCSC Ensembl
Innerchr13:70741385..70775759hg19UCSC Ensembl
Innerchr13:69639386..69673760hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3834375
hg1934375
hg1834375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041687
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)nssv3529347
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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