A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528040



Internal ID15108647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:79559112..79562218hg38UCSC Ensembl
Innerchr9:82174027..82177133hg19UCSC Ensembl
Innerchr9:81363847..81366953hg18UCSC Ensembl
Innerchr9:79403581..79406687hg17UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg383107
hg193107
hg183107
hg173107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704572
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528040
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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