A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437527



Internal ID22495397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154402438..154402633hg38UCSC Ensembl
chrX:153630779..153630974hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871686
Supporting Variants
Samples
Known GenesDNASE1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437527
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