A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445410



Internal ID22503280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123866411..123866594hg38UCSC Ensembl
chrX:123000261..123000444hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883252
Supporting Variants
Samples
Known GenesXIAP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445410
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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