A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029511



Internal ID87366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4654783..4654908hg38UCSC Ensembl
chr10:4696975..4697100hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480819
Supporting Variants
Samples
Known GenesLINC00704
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029511
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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