A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200396



Internal ID22349852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138590426..138590696hg38UCSC Ensembl
chrX:137672587..137672857hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353238, nssv14353239
SamplesHG00731, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200396
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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