A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153126



Internal ID15881119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172711784..172749901hg38UCSC Ensembl
Innerchr5:172138787..172176904hg19UCSC Ensembl
Innerchr5:172071392..172109509hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3838118
hg1938118
hg1838118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600292
Supporting Variants
SamplesNINDS_70
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153126
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