A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562217



Internal ID335176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72106560..72106611hg38UCSC Ensembl
chr10:73866318..73866369hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381276
hg191276
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035304
Samples
Known GenesASCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562217
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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