A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200859



Internal ID22350249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30868515..30868586hg38UCSC Ensembl
chrX:30886632..30886703hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10074n152
Supporting Variantsnssv14350834, nssv14350833, nssv14350835
SamplesHG00732, HG00733, HG00514
Known GenesTAB3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200859
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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