A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527965



Internal ID22397351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80400972..80401165hg38UCSC Ensembl
chr6:81110689..81110882hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14328704
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527965
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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