A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525965



Internal ID22395344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154519722..154519820hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10362n152
Supporting Variantsnssv14354920, nssv14354916, nssv14354919, nssv14354921, nssv14354917, nssv14354915, nssv14354918
SamplesNA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525965
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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