A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14387900



Internal ID22323329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87581448..87581554hg38UCSC Ensembl
chr1:88047131..88047237hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525673
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14387900
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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