A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869447



Internal ID22644382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:62694431..62696320hg38UCSC Ensembl
chrX:61913901..61915790hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg381890
hg191890
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869447
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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