A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458944



Internal ID22516825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37376550..37376550hg38UCSC Ensembl
chrX:37235803..37235803hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963503
Supporting Variants
Samples
Known GenesPRRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458944
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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