A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516416



Internal ID22574379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56918072..56928780hg38UCSC Ensembl
chrX:56944505..56955213hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3810709
hg1910709
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516416
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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