A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872764



Internal ID22647705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147398115..147398218hg38UCSC Ensembl
chrX:146479633..146479736hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872764
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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