A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881979



Internal ID22656956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:108811605..108812314hg38UCSC Ensembl
chrX:108054835..108055544hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881979
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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