A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015595



Internal ID18758129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34342674..34474981hg38UCSC Ensembl
Innerchr9:34342672..34474979hg19UCSC Ensembl
Innerchr9:34332672..34464979hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38132308
hg19132308
hg18132308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688883
Samples
Known GenesC9orf24, DNAI1, FAM219A, KIAA1161, NUDT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015595
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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