A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193559



Internal ID22343992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123783253..123784309hg38UCSC Ensembl
chrX:122917103..122918159hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg381057
hg191057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353426
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193559
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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