A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967232



Internal ID22742167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95929431..95929431hg38UCSC Ensembl
chr6:96377307..96377307hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967232
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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