A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106549



Internal ID22015782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136087940..136089865hg38UCSC Ensembl
chrX:135170099..135172024hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg381926
hg191926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106549
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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