A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516168



Internal ID22574130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:34135111..34138070hg38UCSC Ensembl
chrX:34153228..34156187hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg382960
hg192960
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979494
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516168
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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