A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17393625



Internal ID22451495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234932384..234934691hg38UCSC Ensembl
chr2:235841028..235843335hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg382308
hg192308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888849
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17393625
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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