A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191768



Internal ID22342433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17526957..17527614hg38UCSC Ensembl
chr6:17527188..17527845hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14328239, nssv14328238
SamplesHG00731, HG00732
Known GenesCAP2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191768
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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