A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047175



Internal ID21956409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26397653..26397653hg38UCSC Ensembl
chrX:26415770..26415770hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047175
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