A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517863



Internal ID15445156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95144300..95168945hg38UCSC Ensembl
Innerchr10:96904057..96928702hg19UCSC Ensembl
Innerchr10:96894047..96918692hg18UCSC Ensembl
Innerchr10:96894047..96918692hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3824646
hg1924646
hg1824646
hg1724646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694174
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517863
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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