A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526135



Internal ID22395515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9730207..9730377hg38UCSC Ensembl
chrX:9698247..9698417hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10030n152
Supporting Variantsnssv14351587, nssv14351584, nssv14351583, nssv14351586, nssv14351585, nssv14351588, nssv14351589
SamplesHG00512, NA19238, HG00731, NA19240, HG00733, HG00513, HG00514
Known GenesGPR143
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526135
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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