A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872614



Internal ID22647554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5125737..5125861hg38UCSC Ensembl
chrX:5043778..5043902hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466162
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872614
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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