A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883008



Internal ID22657985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:62548964..62564423hg38UCSC Ensembl
chrX:61768434..61783893hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3815460
hg1915460
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449854
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883008
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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