A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871255



Internal ID22646192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3185845..3185955hg38UCSC Ensembl
chrX:3103886..3103996hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871255
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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