A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216784



Internal ID22362663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7915748..7918602hg38UCSC Ensembl
chr17:7819066..7821920hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382855
hg192855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14388898, nssv14386328
SamplesHG00731, HG00733
Known GenesLOC284023
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216784
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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