A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408746



Internal ID22466616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12541771..12541917hg38UCSC Ensembl
chr2:12681897..12682043hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882584
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408746
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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