A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156177



Internal ID15880646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136837820hg38UCSC Ensembl
Innerchr8:137687955..137850063hg19UCSC Ensembl
Innerchr8:137757137..137919245hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38162109
hg19162109
hg18162109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612400
Supporting Variants
SamplesNINDS_240
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156177
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