A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712708



Internal ID19010989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18471488..18745495hg38UCSC Ensembl
Innerchr13:19045628..19319635hg19UCSC Ensembl
Innerchr13:17943628..18217635hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38274008
hg19274008
hg18274008
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040594
Supporting Variants
Samples
Known GenesLINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712708
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