A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177396



Internal ID22334403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:114471273..114602518hg38UCSC Ensembl
chrX:113705726..113836974hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38131246
hg19131249
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353957, nssv14353958, nssv14353956
SamplesHG00731, HG00732, HG00733
Known GenesHTR2C
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3177396
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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