A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496600



Internal ID273673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110981615..110983431hg38UCSC Ensembl
chr10:112741373..112743189hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041096
Samples
Known GenesSHOC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496600
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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