A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3242073



Internal ID22375159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38728398..38733259hg38UCSC Ensembl
chr6:38696174..38701035hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg384862
hg194862
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14325684, nssv14325685, nssv14325686
SamplesHG00731, HG00732, HG00733
Known GenesDNAH8
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3242073
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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