A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517982



Internal ID15445275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124515244..124546933hg38UCSC Ensembl
Innerchr10:126203813..126235502hg19UCSC Ensembl
Innerchr10:126193803..126225492hg18UCSC Ensembl
Innerchr10:126193803..126225492hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3831690
hg1931690
hg1831690
hg1731690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695394
Samples
Known GenesLHPP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517982
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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