A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15194036



Internal ID21332931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:123389131..123389131hg38UCSC Ensembl
chr12:123873678..123873678hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953279
Supporting Variants
SamplesHG002
Known GenesSETD8
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15194036
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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