A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880313



Internal ID22655283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115307908..115309897hg38UCSC Ensembl
chrX:114542473..114544462hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg381990
hg191990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2294n209
Supporting Variantsnssv17445287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880313
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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