A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065563



Internal ID20632603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93321452..93333361hg38UCSC Ensembl
chr1:93787009..93798918hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3811910
hg1911910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329556
Supporting Variants
Samples
Known GenesLOC100131564
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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