A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111610



Internal ID15618110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40612244..40612660hg38UCSC Ensembl
Innerchr8:40469763..40470179hg19UCSC Ensembl
Innerchr8:40588920..40589336hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38417
hg19417
hg18417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611120
Supporting Variants
Samples
Known GenesZMAT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1111610
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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