A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519427



Internal ID18817708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116974388..117078162hg38UCSC Ensembl
Innerchr11:116845104..116948878hg19UCSC Ensembl
Innerchr11:116350314..116454088hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38103775
hg19103775
hg18103775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050142
Supporting Variants
Samples
Known GenesSIK3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519427
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