A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14296056



Internal ID22161462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219159513..219159588hg38UCSC Ensembl
chr2:220024235..220024310hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205031
Supporting Variants
SamplesHG00514
Known GenesNHEJ1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14296056
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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