A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517023



Internal ID15444316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8715998..8728506hg38UCSC Ensembl
Innerchr8:8573508..8586016hg19UCSC Ensembl
Innerchr8:8610918..8623426hg18UCSC Ensembl
Innerchr8:8610918..8623426hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3812509
hg1912509
hg1812509
hg1712509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653633, nssv691282, nssv670768, nssv667113, nssv692589, nssv659064, nssv682122, nssv661115, nssv666604, nssv667999, nssv658104, nssv665110, nssv663790, nssv657177, nssv681292
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517023
Frequency
Sample Size2026
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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