A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458324



Internal ID22516206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45836197..45836503hg38UCSC Ensembl
chrX:45695624..45695928hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38307
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873692
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458324
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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