A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525473



Internal ID18823754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90195324..90397647hg38UCSC Ensembl
Innerchr13:90847578..91049901hg19UCSC Ensembl
Innerchr13:89645579..89847902hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38202324
hg19202324
hg18202324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046364
Supporting Variants
Samples
Known GenesMIR622
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525473
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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