A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515000



Internal ID18813281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99412928..99541043hg38UCSC Ensembl
Innerchr11:99283659..99411774hg19UCSC Ensembl
Innerchr11:98788869..98916984hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38128116
hg19128116
hg18128116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052546
Supporting Variants
Samples
Known GenesCNTN5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3515000
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