A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035302



Internal ID19124521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135259826..135426111hg38UCSC Ensembl
Innerchr9:138151672..138317957hg19UCSC Ensembl
Innerchr9:137291493..137457778hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38166286
hg19166286
hg18166286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7726n100
Supporting Variantsnssv3759856
Samples
Known GenesC9orf62
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035302
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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