A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969318



Internal ID46868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125606974..125609154hg38UCSC Ensembl
chr6:125928120..125930300hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382181
hg192181
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563709
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969318
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.022791


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