A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611975



Internal ID16399384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114219788..114330448hg38UCSC Ensembl
Innerchr8:115232017..115342677hg19UCSC Ensembl
Innerchr8:115301193..115411853hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38110661
hg19110661
hg18110661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156379
SamplesNINDS_142
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611975
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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