A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052973



Internal ID20620013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150591256..150592790hg38UCSC Ensembl
chr1:150563732..150565266hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381535
hg191535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324089
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052973
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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