A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205037



Internal ID22353795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151649555..151650322hg38UCSC Ensembl
chr6:151970690..151971457hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14331238
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205037
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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