A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525607



Internal ID15452900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126286288..126291252hg38UCSC Ensembl
Innerchr9:129048567..129053531hg19UCSC Ensembl
Innerchr9:128088388..128093352hg18UCSC Ensembl
Innerchr9:126128121..126133085hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384965
hg194965
hg184965
hg174965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701752
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525607
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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