A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459452



Internal ID22517336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68894609..68894677hg38UCSC Ensembl
chrX:68114452..68114520hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873733
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459452
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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