A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022226



Internal ID19111444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:162695..337422hg38UCSC Ensembl
Innerchr9:162695..337422hg19UCSC Ensembl
Innerchr9:152695..327422hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38174728
hg19174728
hg18174728
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7350n100
Supporting Variantsnssv3690973, nssv3758062
Samples
Known GenesC9orf66, CBWD1, DOCK8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022226
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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