A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517782



Internal ID15445075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82364169..82378117hg38UCSC Ensembl
Innerchr10:84123925..84137873hg19UCSC Ensembl
Innerchr10:84113905..84127853hg18UCSC Ensembl
Innerchr10:84113905..84127853hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3813949
hg1913949
hg1813949
hg1713949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676290, nssv653237
Samples
Known GenesNRG3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517782
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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