A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1122300



Internal ID15975486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136844029hg38UCSC Ensembl
Innerchr8:137687955..137856272hg19UCSC Ensembl
Innerchr8:137757137..137925454hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38168318
hg19168318
hg18168318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612405
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1122300
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