A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563973



Internal ID336897
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 StatusM
Merged Variants
Supporting Variantsnssv16984274
Samples
Known GenesMEI4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563973
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer