A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv100n223



Internal ID22803068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16849201..16974000hg38UCSC Ensembl
chr1:17175696..17300495hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38124800
hg19124800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6333329, nsv6332212
Samples
Known GenesCROCC, MIR3675
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv100n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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