A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612376



Internal ID16399785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136670241..136841588hg38UCSC Ensembl
Innerchr8:137682484..137853831hg19UCSC Ensembl
Innerchr8:137751666..137923013hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38171348
hg19171348
hg18171348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1122214
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612376
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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