A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874035



Internal ID22648985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115190653..115190754hg38UCSC Ensembl
chrX:114425216..114425317hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446557
Samples
Known GenesLRCH2, RBMXL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874035
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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