A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101580



Internal ID22010813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49307077..49307183hg38UCSC Ensembl
chrX:49163556..49163662hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649532
Samples
Known GenesGAGE10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101580
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