A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401444



Internal ID22459314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:133854353..133856006hg38UCSC Ensembl
chr2:134611924..134613577hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg381654
hg191654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887555
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401444
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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