A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874778



Internal ID22649731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40661279..40661408hg38UCSC Ensembl
chrX:40520531..40520660hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453366
Samples
Known GenesMED14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874778
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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