A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6516n223



Internal ID22809484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167944501..168316600hg38UCSC Ensembl
chr6:168345181..168717280hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38372100
hg19372100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6600194, nsv6609013, nsv6615812, nsv6601195, nsv6611382, nsv6611398, nsv6615198, nsv6608899, nsv6617771, nsv6604873
Samples
Known GenesDACT2, FRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6516n223
Frequency
Sample Size19652
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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