A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871579



Internal ID22646517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:79056266..79056321hg38UCSC Ensembl
chrX:78311763..78311818hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460111
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871579
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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