A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875082



Internal ID22650037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107601468..107601521hg38UCSC Ensembl
chrX:106844698..106844751hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439989
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875082
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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