A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392427



Internal ID22450297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88897786..89234180hg38UCSC Ensembl
chr2:89197302..89533661hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38336395
hg19336360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881746
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392427
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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