A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203812



Internal ID22352765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151450407..151450486hg38UCSC Ensembl
chr6:151771542..151771621hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14331233
SamplesHG00733
Known GenesRMND1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203812
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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