A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515638



Internal ID22573600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152765605..152767383hg38UCSC Ensembl
chrX:151934121..151935899hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381779
hg191779
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972218
Supporting Variants
Samples
Known GenesMAGEA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515638
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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