A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194488



Internal ID22344797
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355989, nssv14355988
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3194488
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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