A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985396



Internal ID57671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90024787..90024883hg38UCSC Ensembl
chr6:90734506..90734602hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459484
Supporting Variants
Samples
Known GenesBACH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985396
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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