A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064496



Internal ID20631536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87298666..87302129hg38UCSC Ensembl
chr1:87764349..87767812hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg383464
hg193464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064496
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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