A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14306775



Internal ID22258603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42912637..42912637hg38UCSC Ensembl
chr3:42954129..42954129hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3563287
Supporting Variants
SamplesNA19238
Known GenesZNF662
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14306775
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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