A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096932



Internal ID22006165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13300779..13300779hg38UCSC Ensembl
chr10:13342779..13342779hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096932
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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