A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522711



Internal ID15450004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3480671..3500471hg38UCSC Ensembl
Innerchr9:3480671..3500471hg19UCSC Ensembl
Innerchr9:3470671..3490471hg18UCSC Ensembl
Innerchr9:3470671..3490471hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3819801
hg1919801
hg1819801
hg1719801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706124
Samples
Known GenesRFX3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522711
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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