A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229226



Internal ID22371137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79691160..79691339hg38UCSC Ensembl
chr17:77665084..77665269hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38180
hg19186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282529, nssv14282528
SamplesNA19239, HG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229226
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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