A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525449



Internal ID15452742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:83140394..83158573hg38UCSC Ensembl
Innerchr10:84900150..84918329hg19UCSC Ensembl
Innerchr10:84890130..84908309hg18UCSC Ensembl
Innerchr10:84890130..84908309hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3818180
hg1918180
hg1818180
hg1718180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701577
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525449
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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