A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029333



Internal ID19118552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110685..495126hg38UCSC Ensembl
Innerchr9:110685..495126hg19UCSC Ensembl
Innerchr9:100685..485126hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38384442
hg19384442
hg18384442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7346n100
Supporting Variantsnssv3690963
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4, KANK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029333
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