A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213140



Internal ID22360177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85643001..85655200hg38UCSC Ensembl
chr16:85676607..85688806hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3812200
hg1912200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14388082, nssv14373369, nssv14385045, nssv14389898, nssv14389363, nssv14386875, nssv14379024, nssv14387864, nssv14373581
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesGSE1, MIR7851
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213140
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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