A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111103



Internal ID15964289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39386778..39483882hg38UCSC Ensembl
Innerchr8:39244297..39341401hg19UCSC Ensembl
Innerchr8:39363454..39460558hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3897105
hg1997105
hg1897105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611022
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1111103
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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