A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612708



Internal ID16400117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142560330..142590254hg38UCSC Ensembl
Innerchr8:143641691..143671615hg19UCSC Ensembl
Innerchr8:143638693..143668617hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3829925
hg1929925
hg1829925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1124932
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612708
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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