A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515960



Internal ID22573922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20678263..20695446hg38UCSC Ensembl
chrX:20696381..20713564hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3817184
hg1917184
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973502
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515960
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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