A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527324



Internal ID22396709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26194775..26194826hg38UCSC Ensembl
chr15:26439922..26439973hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2858n152
Supporting Variantsnssv14377393, nssv14381328, nssv14390987
SamplesNA19239, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527324
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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