A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015468



Internal ID19104685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115889..273160hg38UCSC Ensembl
Innerchr9:115889..273160hg19UCSC Ensembl
Innerchr9:105889..263160hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38157272
hg19157272
hg18157272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7348n100
Supporting Variantsnssv3690964
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015468
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