A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517562



Internal ID15098169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162060428..162828613hg38UCSC Ensembl
Innerchr6:162481460..163249645hg19UCSC Ensembl
Innerchr6:162401450..163169635hg18UCSC Ensembl
Innerchr6:162451871..163220056hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38768186
hg19768186
hg18768186
hg17768186
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684874, nssv668567, nssv701108, nssv699597, nssv660909, nssv681878, nssv672746, nssv696388, nssv658683, nssv682051, nssv654097, nssv705046, nssv697286, nssv657302, nssv699508, nssv696643, nssv686795, nssv701835, nssv683309, nssv686148, nssv700972, nssv698178, nssv699285, nssv656620, nssv654165, nssv667863, nssv662346, nssv691881, nssv666658, nssv659340, nssv679651, nssv660963, nssv681559, nssv690901, nssv695018, nssv684771, nssv658032, nssv675421, nssv702161, nssv700528, nssv670920, nssv652516, nssv685590, nssv656679, nssv653175, nssv658001, nssv691035, nssv686410, nssv690415, nssv699368, nssv691949, nssv694510, nssv656866, nssv705241, nssv652106, nssv655046, nssv705016, nssv664810, nssv694040, nssv658775
Samples
Known GenesPACRG, PARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517562
Frequency
Sample Size2026
Observed Gain5
Observed Loss55
Observed Complex0
Frequencyn/a


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