A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529101



Internal ID22398494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137952210..137952370hg38UCSC Ensembl
chr6:138273347..138273507hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330310, nssv14330308, nssv14330311, nssv14330306, nssv14330305, nssv14330303, nssv14330309, nssv14330304, nssv14330307
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)nsv3529101
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer