A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969540



Internal ID47008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133833431..133833515hg38UCSC Ensembl
chr6:134154569..134154653hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462945
Supporting Variants
Samples
Known GenesMGC34034
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969540
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.601445


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