A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035328



Internal ID91290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77864100..77866931hg38UCSC Ensembl
chr10:79623858..79626689hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382832
hg192832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493855
Supporting Variants
Samples
Known GenesDLG5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035328
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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