A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024729



Internal ID18767260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39053783..39273079hg38UCSC Ensembl
Innerchr9:39053780..39273076hg19UCSC Ensembl
Innerchr9:39043780..39263076hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38219297
hg19219297
hg18219297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7530n100
Supporting Variantsnssv3688932
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)nsv1024729
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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