A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528559



Internal ID15455852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135992854..135997730hg38UCSC Ensembl
Innerchr9:138884700..138889576hg19UCSC Ensembl
Innerchr9:138024521..138029397hg18UCSC Ensembl
Innerchr9:136110645..136115521hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg384877
hg194877
hg184877
hg174877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705175
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528559
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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