A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871241



Internal ID22646178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115190653..115191015hg38UCSC Ensembl
chrX:114425216..114425578hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443921
Samples
Known GenesLRCH2, RBMXL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871241
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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