A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524697



Internal ID15451990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:73434627..73436421hg38UCSC Ensembl
Innerchr8:74346862..74348656hg19UCSC Ensembl
Innerchr8:74509416..74511210hg18UCSC Ensembl
Innerchr8:74509416..74511210hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381795
hg191795
hg181795
hg171795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700676
Samples
Known GenesSTAU2, STAU2-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524697
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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