A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2965n223



Internal ID22805933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:835045..1069726hg38UCSC Ensembl
chr17:738285..972966hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38234682
hg19234682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6509810, nsv6512060, nsv6499081
Samples
Known GenesABR, MIR3183, NXN, TIMM22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2965n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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