A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015260



Internal ID19104477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101857..348466hg38UCSC Ensembl
Innerchr9:101857..348466hg19UCSC Ensembl
Innerchr9:91857..338466hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38246610
hg19246610
hg18246610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7347n100
Supporting Variantsnssv3690961
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015260
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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