A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357502



Internal ID22210553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28131507..28131997hg38UCSC Ensembl
chr1:28458018..28458508hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198915
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357502
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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