A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036781



Internal ID92270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86970565..86970634hg38UCSC Ensembl
chr10:88730322..88730391hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476388
Supporting Variants
Samples
Known GenesADIRF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036781
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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