A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460479



Internal ID22518362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26397653..26397653hg38UCSC Ensembl
chrX:26415770..26415770hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954267
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460479
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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