A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877576



Internal ID22652541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:106683464..106695365hg38UCSC Ensembl
chrX:105926694..105938595hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3811902
hg1911902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447743
Samples
Known GenesRNF128
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877576
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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