A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355988



Internal ID22283669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22230948..22231138hg38UCSC Ensembl
chr1:22557441..22557631hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194488
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355988
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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