A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105446



Internal ID20672486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9504122..9504577hg38UCSC Ensembl
chr3:9545806..9546261hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375281
Supporting Variants
Samples
Known GenesLHFPL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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