A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515637



Internal ID22573599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152700649..152702089hg38UCSC Ensembl
chrX:151869127..151870567hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381441
hg191441
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970957
Supporting Variants
Samples
Known GenesMAGEA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515637
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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