A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525614



Internal ID18823895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112600099..112624039hg38UCSC Ensembl
Innerchr13:113254413..113278353hg19UCSC Ensembl
Innerchr13:112302414..112326354hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3823941
hg1923941
hg1823941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052539
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)nssv3525614
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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