A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039044



Internal ID93776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127070313..127071445hg38UCSC Ensembl
chr10:128868577..128869709hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg381133
hg191133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512039
Supporting Variants
Samples
Known GenesDOCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039044
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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