A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026304



Internal ID18768836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142143283..142212197hg38UCSC Ensembl
Innerchr8:143224644..143293558hg19UCSC Ensembl
Innerchr8:143222551..143291465hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3868915
hg1968915
hg1868915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7332n100
Supporting Variantsnssv3690086
Samples
Known GenesLINC00051, MIR4472-1, TSNARE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026304
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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