A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397881



Internal ID22455751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88860605..89234184hg38UCSC Ensembl
chr2:89160117..89533665hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38373580
hg19373549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887238
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397881
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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