A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515274



Internal ID22573233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120873463..120875568hg38UCSC Ensembl
chrX:120007317..120009422hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg382106
hg192106
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977551
Supporting Variants
Samples
Known GenesCT47B1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515274
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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