A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14350275



Internal ID22277433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38497636..38497880hg38UCSC Ensembl
chrX:38356889..38357133hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201783
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14350275
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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