A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875155



Internal ID22650111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113164712..113165300hg38UCSC Ensembl
chrX:112407939..112408527hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875155
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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