A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208811



Internal ID22356992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47090909..47090961hg38UCSC Ensembl
chrX:46950308..46950360hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10111n152
Supporting Variantsnssv14351113, nssv14351114, nssv14351112
SamplesHG00732, NA19240, HG00514
Known GenesRGN
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208811
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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