A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041990



Internal ID19131209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135259826..135420175hg38UCSC Ensembl
Innerchr9:138151672..138312021hg19UCSC Ensembl
Innerchr9:137291493..137451842hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38160350
hg19160350
hg18160350
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7726n100
Supporting Variantsnssv3696494, nssv3696493
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)nsv1041990
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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