A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517136



Internal ID15444429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:62303056..62310322hg38UCSC Ensembl
Innerchr8:63215615..63222881hg19UCSC Ensembl
Innerchr8:63378169..63385435hg18UCSC Ensembl
Innerchr8:63378169..63385435hg17UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg387267
hg197267
hg187267
hg177267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668826, nssv666886, nssv668194, nssv692137, nssv656716, nssv692042, nssv672340, nssv660856, nssv692393, nssv659212, nssv658275, nssv680949, nssv668073, nssv693971, nssv658688, nssv653841, nssv669206, nssv659792, nssv682076, nssv654337, nssv667167, nssv672099, nssv660947, nssv685324, nssv676332, nssv671384, nssv656373, nssv669988, nssv687468, nssv653876, nssv693122
Samples
Known GenesNKAIN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517136
Frequency
Sample Size2026
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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