A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878775



Internal ID22653740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125321662..125321724hg38UCSC Ensembl
chrX:124455511..124455573hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437573
Samples
Known GenesLOC100129520
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878775
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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