A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099705



Internal ID20666745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177516934..177522957hg38UCSC Ensembl
chr3:177234722..177240745hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg386024
hg196024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357362
Supporting Variants
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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