A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523871



Internal ID15104478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91934497..91934826hg38UCSC Ensembl
Innerchr9:94696779..94697108hg19UCSC Ensembl
Innerchr9:93736600..93736929hg18UCSC Ensembl
Innerchr9:91776334..91776663hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38330
hg19330
hg18330
hg17330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699712
Samples
Known GenesROR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523871
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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