A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038821



Internal ID19128040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135259826..135418642hg38UCSC Ensembl
Innerchr9:138151672..138310488hg19UCSC Ensembl
Innerchr9:137291493..137450309hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38158817
hg19158817
hg18158817
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7726n100
Supporting Variantsnssv3696492, nssv3696490, nssv3696489, nssv3696491
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)nsv1038821
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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