A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515297



Internal ID22573257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125100051..125102479hg38UCSC Ensembl
chrX:124233900..124236328hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg382429
hg192429
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968079
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515297
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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