A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963437



Internal ID22738372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71375099..71375099hg38UCSC Ensembl
chr6:72084802..72084802hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434970
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963437
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