A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111098



Internal ID15964284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380500..39386523hg38UCSC Ensembl
Innerchr8:39238019..39244042hg19UCSC Ensembl
Innerchr8:39357176..39363199hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg386024
hg196024
hg186024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611017
Supporting Variants
Samples
Known GenesADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1111098
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