A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880027



Internal ID22654997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107098377..107099524hg38UCSC Ensembl
chrX:106341607..106342754hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg381148
hg191148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431071
Samples
Known GenesRBM41
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880027
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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