A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035304



Internal ID91272
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 StatusS
Merged Variantsnsv5562217
Supporting Variants
Samples
Known GenesASCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035304
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002031


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