A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419752



Internal ID22477622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151776896..151778954hg38UCSC Ensembl
chr3:151494684..151496742hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382059
hg192059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902703
Supporting Variants
Samples
Known GenesLOC201651, MIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419752
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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