A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402591



Internal ID22460461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88861885..89244779hg38UCSC Ensembl
chr2:89161397..89544262hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38382895
hg19382866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871646
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402591
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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