A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878144



Internal ID22653108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45521142..45522192hg38UCSC Ensembl
chrX:45380387..45381437hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381051
hg191051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461467
Samples
Known GenesLOC101927528
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878144
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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