A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392317



Internal ID22450187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9145351..9154304hg38UCSC Ensembl
chr2:9285480..9294433hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg388954
hg198954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873391
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392317
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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