A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219869



Internal ID22364747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79709620..79709883hg38UCSC Ensembl
chr17:77683428..77683691hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282541, nssv14282540
SamplesHG00731, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219869
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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