A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520007



Internal ID15100614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39004143..39184068hg38UCSC Ensembl
Innerchr9:39004140..39184065hg19UCSC Ensembl
Innerchr9:38994140..39174065hg18UCSC Ensembl
Innerchr9:38994140..39174065hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38179926
hg19179926
hg18179926
hg17179926
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675894, nssv675190, nssv688627, nssv686079, nssv660070, nssv706055
Samples
Known GenesCNTNAP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520007
Frequency
Sample Size2026
Observed Gain3
Observed Loss3
Observed Complex0
Frequencyn/a


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