A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097128



Internal ID20664168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169774088..169776925hg38UCSC Ensembl
chr3:169491876..169494713hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg382838
hg192838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372501
Supporting Variants
Samples
Known GenesMYNN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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