A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044512



Internal ID19133731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135259826..135402220hg38UCSC Ensembl
Innerchr9:138151672..138294066hg19UCSC Ensembl
Innerchr9:137291493..137433887hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38142395
hg19142395
hg18142395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7726n100
Supporting Variantsnssv3759842, nssv3759843, nssv3696443, nssv3759844, nssv3696444
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)nsv1044512
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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