A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208139



Internal ID22356428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34035496..34035562hg38UCSC Ensembl
chr6:34003273..34003339hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14324892, nssv14324891
SamplesHG00512, HG00514
Known GenesGRM4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208139
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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