A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611748



Internal ID16399157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:93269212..93302887hg38UCSC Ensembl
Innerchr8:94281440..94315115hg19UCSC Ensembl
Innerchr8:94350616..94384291hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3833676
hg1933676
hg1833676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117841
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611748
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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