A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985077



Internal ID57445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91679325..91679376hg38UCSC Ensembl
chr6:92389043..92389094hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546734
Supporting Variants
Samples
Known GenesCASC6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985077
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.046519


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