A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529731



Internal ID22399122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36500697..36501010hg38UCSC Ensembl
chr6:36468474..36468787hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14325595, nssv14325599, nssv14325596, nssv14325594, nssv14325597, nssv14325598
SamplesNA19238, NA19239, HG00732, NA19240, HG00513, HG00514
Known GenesSTK38
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529731
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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