A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14290745



Internal ID22284828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73903939..73904249hg38UCSC Ensembl
chr2:74131066..74131376hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3195132
Supporting Variants
SamplesNA19239
Known GenesACTG2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14290745
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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