A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519668



Internal ID18817949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50322134..50810134hg38UCSC Ensembl
Innerchr11:50281305..50769305hg19UCSC Ensembl
Innerchr11:50237881..50725881hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38488001
hg19488001
hg18488001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048846
Supporting Variants
Samples
Known GenesLOC646813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519668
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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