A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111182



Internal ID15964368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39406879..39507504hg38UCSC Ensembl
Innerchr8:39264398..39365023hg19UCSC Ensembl
Innerchr8:39383555..39484180hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38100626
hg19100626
hg18100626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611046
Supporting Variants
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1111182
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer