A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267062



Internal ID20476280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85254301..85254635hg38UCSC Ensembl
chrX:84509307..84509641hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766176
Supporting Variants
Samples
Known GenesZNF711
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267062
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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