A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105364



Internal ID22014597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73870894..73870960hg38UCSC Ensembl
chrX:73090729..73090795hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639134
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105364
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