A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516699



Internal ID15443992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130186696..130846770hg38UCSC Ensembl
Innerchr10:131984960..132645033hg19UCSC Ensembl
Innerchr10:131874950..132535023hg18UCSC Ensembl
Innerchr10:131874950..132535023hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38660075
hg19660074
hg18660074
hg17660074
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700905, nssv704291, nssv686990, nssv700904, nssv696367, nssv673466, nssv696366, nssv670527, nssv691362, nssv696781, nssv692771, nssv670221, nssv703515
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516699
Frequency
Sample Size2026
Observed Gain9
Observed Loss4
Observed Complex0
Frequencyn/a


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