A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517526



Internal ID15444819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81118732..81154273hg38UCSC Ensembl
Innerchr10:82878488..82914029hg19UCSC Ensembl
Innerchr10:82868468..82904009hg18UCSC Ensembl
Innerchr10:82868468..82904009hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3835542
hg1935542
hg1835542
hg1735542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691691, nssv678565, nssv658450, nssv663038, nssv681428, nssv669827, nssv691180, nssv673663, nssv670382, nssv669637, nssv684004, nssv687573, nssv678313, nssv683987, nssv695839, nssv675690, nssv675591, nssv678983, nssv682920, nssv683703, nssv674801, nssv670550, nssv683428, nssv661347, nssv673019, nssv673631, nssv680183, nssv677050, nssv652739, nssv676140, nssv658554, nssv689728, nssv686973, nssv667045, nssv680446, nssv660117, nssv690544, nssv674115, nssv669466, nssv668893, nssv663536, nssv670931, nssv681475, nssv672401, nssv688569, nssv670979, nssv654603, nssv661098, nssv653090, nssv680641, nssv672853, nssv662483, nssv668485, nssv652276, nssv666091, nssv663144, nssv662242, nssv662959, nssv681353
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517526
Frequency
Sample Size2026
Observed Gain0
Observed Loss59
Observed Complex0
Frequencyn/a


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