A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978040



Internal ID52765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3634939..3635094hg38UCSC Ensembl
chr6:3635173..3635328hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978040
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.018264


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