A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214886



Internal ID22361396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25999825..25999895hg38UCSC Ensembl
chr15:26244972..26245042hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2856n152
Supporting Variantsnssv14373097, nssv14390825, nssv14378966, nssv14386316
SamplesHG00512, NA19240, HG00513, HG00514
Known GenesLOC100128714
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214886
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer