A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211835



Internal ID22359266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127362837..127363019hg38UCSC Ensembl
chr10:129161101..129161283hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355998, nssv14355997, nssv14355990, nssv14355993, nssv14355995, nssv14355991, nssv14355994, nssv14355992, nssv14355996
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesDOCK1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211835
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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