A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092096



Internal ID20659136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11163831..11178119hg38UCSC Ensembl
chr3:11205517..11219805hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3814289
hg1914289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373557
Supporting Variants
Samples
Known GenesHRH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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