A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226994



Internal ID22369617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112714951..112724650hg38UCSC Ensembl
chr13:113369265..113378964hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2467n152
Supporting Variantsnssv14372063, nssv14372068, nssv14372071, nssv14372065, nssv14372064, nssv14372067, nssv14372066, nssv14372069, nssv14372070
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesATP11A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226994
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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