A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1098099



Internal ID15951285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148377131..148378940hg38UCSC Ensembl
Innerchr7:148074223..148076032hg19UCSC Ensembl
Innerchr7:147705156..147706965hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg381810
hg191810
hg181810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608967
Supporting Variants
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1098099
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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