A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526828



Internal ID22396211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:79864707..79864784hg38UCSC Ensembl
chrX:79120207..79120284hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352367, nssv14352365, nssv14352366
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526828
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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