A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984274



Internal ID56893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77805862..77805913hg38UCSC Ensembl
chr6:78515579..78515630hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg383276
hg193276
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563973
Supporting Variants
Samples
Known GenesMEI4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984274
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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