A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397077



Internal ID22454947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134643144..134643208hg38UCSC Ensembl
chr3:134361986..134362050hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896286
Supporting Variants
Samples
Known GenesKY
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397077
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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