A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190840



Internal ID22341642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57608942..57609000hg38UCSC Ensembl
chrX:57635375..57635433hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10138n152
Supporting Variantsnssv14351836, nssv14351835, nssv14351837
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190840
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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