A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887433



Internal ID22662425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37991457..37995172hg38UCSC Ensembl
chrX:37850710..37854425hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg383716
hg193716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454612
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887433
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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