A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023246



Internal ID18765778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33181636..33261063hg38UCSC Ensembl
Innerchr9:33181634..33261061hg19UCSC Ensembl
Innerchr9:33171634..33251061hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3879428
hg1979428
hg1879428
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688875
Samples
Known GenesBAG1, SPINK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023246
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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