A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3113n223



Internal ID22806081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41223401..41240500hg38UCSC Ensembl
chr17:39379653..39396752hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3817100
hg1917100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6496151, nsv6511876, nsv6514988
Samples
Known GenesKRTAP9-2, KRTAP9-3, KRTAP9-8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3113n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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