A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985869



Internal ID57992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88128904..88157547hg38UCSC Ensembl
chr6:88838623..88867266hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3828644
hg1928644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471962
Supporting Variants
Samples
Known GenesCNR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985869
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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