A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612424



Internal ID16399833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675987..136866822hg38UCSC Ensembl
Innerchr8:137688230..137879065hg19UCSC Ensembl
Innerchr8:137757412..137948247hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38190836
hg19190836
hg18190836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1156194
Samples1780854566_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612424
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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