A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404063



Internal ID22461933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:59161360..59175834hg38UCSC Ensembl
chr2:59388495..59402969hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3814475
hg1914475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874808
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404063
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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