A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527116



Internal ID22396500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146812356..146819263hg38UCSC Ensembl
chr6:147133492..147140399hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg386908
hg196908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14331113, nssv14331114
SamplesNA19238, HG00733
Known GenesADGB
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527116
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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