A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525549



Internal ID22394927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46935144..46936222hg38UCSC Ensembl
chrX:46794579..46795657hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351105, nssv14351104
SamplesNA19238, NA19240
Known GenesJADE3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525549
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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