A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203175



Internal ID20770215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92699438..92766081hg38UCSC Ensembl
chr1:93164995..93231638hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3866644
hg1966644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330317
Supporting Variants
Samples
Known GenesEVI5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203175
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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