A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6468n223



Internal ID22809436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160020701..160144000hg38UCSC Ensembl
chr6:160441733..160565032hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38123300
hg19123300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6604792, nsv6615059, nsv6619029
Samples
Known GenesIGF2R, LOC729603, SLC22A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6468n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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