A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984836



Internal ID57276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47101266..47101324hg38UCSC Ensembl
chr6:47069002..47069060hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460431
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984836
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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