A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525888



Internal ID15106495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:129309677..129410480hg38UCSC Ensembl
Innerchr10:131107941..131208744hg19UCSC Ensembl
Innerchr10:130997931..131098734hg18UCSC Ensembl
Innerchr10:130997931..131098734hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38100804
hg19100804
hg18100804
hg17100804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv53n21
Supporting Variantsnssv702091
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525888
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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