A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201134



Internal ID22350483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116392314..116393412hg38UCSC Ensembl
chrX:115523458..115524560hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg381099
hg191103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354009, nssv14354010
SamplesHG00732, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201134
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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