A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611425



Internal ID16398834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:61051140..61113389hg38UCSC Ensembl
Innerchr8:61963699..62025948hg19UCSC Ensembl
Innerchr8:62126253..62188502hg18UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg3862250
hg1962250
hg1862250
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156845
Samples1780854061_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611425
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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