A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015962



Internal ID19105180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64507199..64954062hg38UCSC Ensembl
Innerchr9:69519617..69966480hg19UCSC Ensembl
Innerchr9:68809437..69256300hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38446864
hg19446864
hg18446864
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7657n100
Supporting Variantsnssv3696154
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015962
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