A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351763



Internal ID22264185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37495238..37508745hg38UCSC Ensembl
chrX:37354491..37367998hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3813508
hg1913508
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526479
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351763
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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