A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521768



Internal ID15449061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78644279..78656545hg38UCSC Ensembl
Innerchr9:81259195..81271461hg19UCSC Ensembl
Innerchr9:80449015..80461281hg18UCSC Ensembl
Innerchr9:78488749..78501015hg17UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3812267
hg1912267
hg1812267
hg1712267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694535
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521768
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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