A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191436



Internal ID22342142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45940549..45940601hg38UCSC Ensembl
chrX:45799984..45800036hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10106n152
Supporting Variantsnssv14351095, nssv14351096
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191436
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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