A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611808



Internal ID16399217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:98532537..98579508hg38UCSC Ensembl
Innerchr8:99544765..99591736hg19UCSC Ensembl
Innerchr8:99613941..99660912hg18UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3846972
hg1946972
hg1846972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1118155
Samples
Known GenesSTK3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611808
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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