A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517013



Internal ID22574976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:99924427..99938788hg38UCSC Ensembl
chrX:99179425..99193786hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3814362
hg1914362
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973785
Supporting Variants
Samples
Known GenesXRCC6P5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517013
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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