A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035055



Internal ID18777586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38989369..39273079hg38UCSC Ensembl
Innerchr9:38989366..39273076hg19UCSC Ensembl
Innerchr9:38979366..39263076hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38283711
hg19283711
hg18283711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7524n100
Supporting Variantsnssv3688909
Samples
Known GenesCNTNAP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035055
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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