A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453216



Internal ID22511090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:34024873..34054732hg38UCSC Ensembl
chrX:34042990..34072849hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3829860
hg1929860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886289
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453216
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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