A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914922



Internal ID10706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61627611..61629701hg38UCSC Ensembl
chr2:61854746..61856836hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg382091
hg192091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449956
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914922
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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