A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525553



Internal ID18823834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104772904..104797192hg38UCSC Ensembl
Innerchr13:105425255..105449543hg19UCSC Ensembl
Innerchr13:104223256..104247544hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3824289
hg1924289
hg1824289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049107
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)nssv3525553
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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