A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408475



Internal ID22466345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18718596..18725551hg38UCSC Ensembl
chr2:18899862..18906817hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg386956
hg196956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881164
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408475
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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