A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195670



Internal ID22345806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163611643..163611711hg38UCSC Ensembl
chr6:164032675..164032743hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14331367
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195670
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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