A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611121



Internal ID16051844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40679117..40711485hg38UCSC Ensembl
Innerchr8:40536636..40569004hg19UCSC Ensembl
Innerchr8:40655793..40688161hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3832369
hg1932369
hg1832369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1111613
Samples
Known GenesZMAT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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