A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049679



Internal ID19138898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34349728..34499613hg38UCSC Ensembl
Innerchr13:34923865..35073750hg19UCSC Ensembl
Innerchr13:33821865..33971750hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38149886
hg19149886
hg18149886
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523241
Samples
Known GenesLINC00457
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049679
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