A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134079



Internal ID15640579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39004143..39444669hg38UCSC Ensembl
Innerchr9:39004140..39444668hg19UCSC Ensembl
Innerchr9:38994140..39434668hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38440527
hg19440529
hg18440529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614284
Supporting Variants
Samples
Known GenesCNTNAP3, LOC653501, SPATA31A1, SPATA31A2, ZNF658B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1134079
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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