A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970135



Internal ID47420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137575965..137645185hg38UCSC Ensembl
chr6:137897102..137966322hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3869221
hg1969221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970135
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001562


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