A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419125



Internal ID22476995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180403256..180413580hg38UCSC Ensembl
chr3:180121044..180131368hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3810325
hg1910325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894229
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419125
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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