A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521371



Internal ID18819652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126682920..126881245hg38UCSC Ensembl
Innerchr10:128371489..128569814hg19UCSC Ensembl
Innerchr10:128361479..128559804hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38198326
hg19198326
hg18198326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052968
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3521371
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer