A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433092



Internal ID22490962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110070789..110094561hg38UCSC Ensembl
chrX:109314017..109337789hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3823773
hg1923773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882109
Supporting Variants
Samples
Known GenesMIR3978, TMEM164
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433092
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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