A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019326



Internal ID18761860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39053783..39315027hg38UCSC Ensembl
Innerchr9:39053780..39315024hg19UCSC Ensembl
Innerchr9:39043780..39305024hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38261245
hg19261245
hg18261245
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688934, nssv3688935
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)nsv1019326
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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