A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047178



Internal ID99295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74860749..74860817hg38UCSC Ensembl
chr11:74571794..74571862hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512908
Supporting Variants
Samples
Known GenesXRRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047178
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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