A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915744



Internal ID11226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79272859..79273014hg38UCSC Ensembl
chr2:79499985..79500140hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915744
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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