A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111096



Internal ID15964282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380149..39567509hg38UCSC Ensembl
Innerchr8:39237668..39425028hg19UCSC Ensembl
Innerchr8:39356825..39544185hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38187361
hg19187361
hg18187361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611016
Supporting Variants
Samples
Known GenesADAM3A, ADAM5, LOC100130964
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1111096
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