A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1110522



Internal ID15963708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380149..39480405hg38UCSC Ensembl
Innerchr8:39237668..39337924hg19UCSC Ensembl
Innerchr8:39356825..39457081hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38100257
hg19100257
hg18100257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611004
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)nssv1110522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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