A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035196



Internal ID18777727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135878111..135946459hg38UCSC Ensembl
Innerchr9:138769957..138838305hg19UCSC Ensembl
Innerchr9:137909778..137978126hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3868349
hg1968349
hg1868349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7728n100
Supporting Variantsnssv3696507
Samples
Known GenesCAMSAP1, UBAC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035196
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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