A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065135



Internal ID20632175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91451441..91488623hg38UCSC Ensembl
chr1:91916998..91954180hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3837183
hg1937183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326825
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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