A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353958



Internal ID22233995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:114471273..114602518hg38UCSC Ensembl
chrX:113705726..113836974hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38131246
hg19131249
Variant TypeOTHER complex substitution
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3177396
Supporting Variants
SamplesHG00733
Known GenesHTR2C
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353958
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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