A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037744



Internal ID92911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106286136..106418495hg38UCSC Ensembl
chr10:108045894..108178253hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38132360
hg19132360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037744
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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