A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963503



Internal ID22738438
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 StatusM
Merged Variants
Supporting Variantsnssv17458944
Samples
Known GenesPRRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963503
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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