A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879490



Internal ID22654459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92125868..92143866hg38UCSC Ensembl
chrX:91380867..91398865hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3817999
hg1917999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457980
Samples
Known GenesPCDH11X
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879490
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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