A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611424



Internal ID16398833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60945654..60957888hg38UCSC Ensembl
Innerchr8:61858213..61870447hg19UCSC Ensembl
Innerchr8:62020767..62033001hg18UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg3812235
hg1912235
hg1812235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12181n54
Supporting Variantsnssv1115648
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611424
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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