A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742010



Internal ID165676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112196500..112335100hg38UCSC Ensembl
chrX:111439728..111578328hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38138601
hg19138601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138204
Supporting Variants
Samples
Known GenesZCCHC16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742010
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00292703


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