A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643607



Internal ID21835654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:114700628..114700744hg38UCSC Ensembl
chrX:113935044..113935160hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102735
Supporting Variants
Samples
Known GenesHTR2C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643607
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