A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046364



Internal ID19135583
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 StatusM
Merged Variantsdgv1728n100
Supporting Variantsnssv3525473
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)nsv1046364
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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