A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031342



Internal ID19120564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:525752..814210hg38UCSC Ensembl
Innerchr9:525752..814210hg19UCSC Ensembl
Innerchr9:515752..804210hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38288459
hg19288459
hg18288459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7363n100
Supporting Variantsnssv3758073, nssv3691036
Samples
Known GenesKANK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031342
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