A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985276



Internal ID57582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85511443..85512060hg38UCSC Ensembl
chr6:86221161..86221778hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457086
Supporting Variants
Samples
Known GenesSNX14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985276
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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