A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033964



Internal ID19123186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:525037..816742hg38UCSC Ensembl
Innerchr9:525037..816742hg19UCSC Ensembl
Innerchr9:515037..806742hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38291706
hg19291706
hg18291706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7363n100
Supporting Variantsnssv3691033
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)nsv1033964
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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