A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867815



Internal ID22642750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48574570..48575163hg38UCSC Ensembl
chrX:48432958..48433551hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464237
Samples
Known GenesRBM3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867815
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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