A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985283



Internal ID57588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85619907..85619963hg38UCSC Ensembl
chr6:86329625..86329681hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470925
Supporting Variants
Samples
Known GenesSYNCRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985283
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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