A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468313



Internal ID22526202
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 StatusS
Merged Variantsnsv5882916
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468313
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003


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