A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515987



Internal ID22573949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2282213..2324425hg38UCSC Ensembl
chrX:2200254..2242466hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3842213
hg1942213
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974124
Supporting Variants
Samples
Known GenesDHRSX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515987
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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