A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423702



Internal ID22481572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154288183..154288744hg38UCSC Ensembl
chr3:154005972..154006533hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896853
Supporting Variants
Samples
Known GenesDHX36
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423702
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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