A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526330



Internal ID22395710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:143750269..143750392hg38UCSC Ensembl
chrX:142833364..142833487hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353386
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526330
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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