A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989402



Internal ID60360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152120640..152124653hg38UCSC Ensembl
chr6:152441775..152445788hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384014
hg194014
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556982
Supporting Variants
Samples
Known GenesSYNE1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989402
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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