A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14298838



Internal ID22301622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241487667..241488435hg38UCSC Ensembl
chr2:242427082..242427850hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204302
Supporting Variants
SamplesNA19240
Known GenesFARP2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14298838
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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