A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394278



Internal ID22452148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88832771..89213422hg38UCSC Ensembl
chr2:89132284..89512907hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38380652
hg19380624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869871
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394278
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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