A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398457



Internal ID22456327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224296670..224302042hg38UCSC Ensembl
chr2:225161387..225166759hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg385373
hg195373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898171
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398457
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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