A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515962



Internal ID22573924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21251053..21255932hg38UCSC Ensembl
chrX:21269171..21274050hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg384880
hg194880
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515962
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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