A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869064



Internal ID22644000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56495260..56540274hg38UCSC Ensembl
chrX:56521693..56566707hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3845015
hg1945015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461731
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869064
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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