A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3395n152



Internal ID22819098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:413795..413858hg38UCSC Ensembl
chr17:263586..263649hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3286988, nsv3285187
SamplesNA19240, HG00514
Known GenesC17orf97
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv3395n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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