A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882916



Internal ID22657893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65772967..65773070hg38UCSC Ensembl
chrX:64992809..64992912hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882916
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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