A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065655



Internal ID20632695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94786401..94788500hg38UCSC Ensembl
chr1:95251957..95254056hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331219
Supporting Variants
Samples
Known GenesLINC01057
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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