A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881430



Internal ID22656405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23523498..23628887hg38UCSC Ensembl
chrX:23541615..23647004hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38105390
hg19105390
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457915
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881430
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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