A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1111101



Internal ID15964287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39381083..39529660hg38UCSC Ensembl
Innerchr8:39238602..39387179hg19UCSC Ensembl
Innerchr8:39357759..39506336hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38148578
hg19148578
hg18148578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611020
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)nssv1111101
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