A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909877



Internal ID7355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5946186..5947372hg38UCSC Ensembl
chr2:6086318..6087504hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg381187
hg191187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448732
Supporting Variants
Samples
Known GenesLINC01105
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909877
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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