A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022560



Internal ID82727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72842517..72851543hg38UCSC Ensembl
chr9:75457433..75466459hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg389027
hg199027
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147246
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022560
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002029


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