A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029024



Internal ID87045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6824314..6832809hg38UCSC Ensembl
chr10:6866276..6874771hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg388496
hg198496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489932
Supporting Variants
Samples
Known GenesLINC00707
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029024
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001719


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