A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022158



Internal ID19111376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63968448..64617909hg38UCSC Ensembl
Innerchr9:69186118..69630327hg19UCSC Ensembl
Innerchr9:68475938..68920147hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38649462
hg19444210
hg18444210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7653n100
Supporting Variantsnssv3696085, nssv3696084, nssv3696086
Samples
Known GenesANKRD20A4, CBWD5, CBWD6, FOXD4L6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022158
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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