A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872135



Internal ID22647074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:143986148..144002593hg38UCSC Ensembl
chrX:143069254..143085699hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3816446
hg1916446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872135
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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