A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982645



Internal ID55793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54209628..54210738hg38UCSC Ensembl
chr6:54074426..54075536hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg381111
hg191111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462383
Supporting Variants
Samples
Known GenesMLIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982645
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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