A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516930



Internal ID15444223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82928996..82956767hg38UCSC Ensembl
Innerchr10:84688752..84716523hg19UCSC Ensembl
Innerchr10:84678732..84706503hg18UCSC Ensembl
Innerchr10:84678732..84706503hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3827772
hg1927772
hg1827772
hg1727772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658204, nssv685551, nssv675558, nssv671635, nssv690385, nssv663298, nssv686331, nssv667262, nssv691842, nssv670642, nssv676955, nssv660881, nssv679919, nssv659466, nssv680931, nssv681732, nssv656667, nssv662960, nssv659520, nssv653477, nssv660925, nssv672041, nssv675080, nssv689032, nssv673430, nssv658865, nssv690093
Samples
Known GenesNRG3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516930
Frequency
Sample Size2026
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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