A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524089



Internal ID15451382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:112748914..112840548hg38UCSC Ensembl
Innerchr8:113761143..113852777hg19UCSC Ensembl
Innerchr8:113830319..113921953hg18UCSC Ensembl
Innerchr8:113830319..113921953hg17UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3891635
hg1991635
hg1891635
hg1791635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699961
Samples
Known GenesCSMD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524089
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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