A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884709



Internal ID22659692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16454054..16461126hg38UCSC Ensembl
chrX:16472177..16479249hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg387073
hg197073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884709
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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