A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065231



Internal ID20632271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98114426..98115336hg38UCSC Ensembl
chr1:98579982..98580892hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330036
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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