A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874629



Internal ID22649583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92112536..92113795hg38UCSC Ensembl
chrX:91367535..91368794hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg381260
hg191260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454415
Samples
Known GenesPCDH11X
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874629
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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