A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423165



Internal ID22481035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72045399..72045466hg38UCSC Ensembl
chr3:72094550..72094617hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892962
Supporting Variants
Samples
Known GenesLINC00877
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423165
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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