A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191272



Internal ID22341999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:906315..906438hg38UCSC Ensembl
chr6:906898..907026hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38124
hg19129
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14324706, nssv14324709, nssv14324707, nssv14324703, nssv14324705, nssv14324708, nssv14324702, nssv14324704, nssv14324710
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191272
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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