A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882170



Internal ID22657147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25929822..25930155hg38UCSC Ensembl
chrX:25947939..25948272hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455130
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882170
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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