A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914778



Internal ID10600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77001423..77006449hg38UCSC Ensembl
chr2:77228549..77233575hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg385027
hg195027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450060
Supporting Variants
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914778
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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