A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873699



Internal ID22648647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:143750339..143750388hg38UCSC Ensembl
chrX:142833434..142833483hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433243
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873699
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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