A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389890



Internal ID22447760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219589071..219592181hg38UCSC Ensembl
chr2:220453793..220456903hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg383111
hg193111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897648
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389890
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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