A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520369



Internal ID15447662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110447119..110465955hg38UCSC Ensembl
Innerchr10:112206877..112225713hg19UCSC Ensembl
Innerchr10:112196867..112215703hg18UCSC Ensembl
Innerchr10:112196867..112215703hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3818837
hg1918837
hg1818837
hg1718837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694496, nssv663259, nssv673044
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520369
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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