A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409639



Internal ID22467509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151759846..151762251hg38UCSC Ensembl
chr3:151477634..151480039hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382406
hg192406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896366
Supporting Variants
Samples
Known GenesMIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409639
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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