A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462926



Internal ID22520811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:62694431..62696320hg38UCSC Ensembl
chrX:61913901..61915790hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg381890
hg191890
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462926
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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