A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617771



Internal ID20990842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167974901..168316300hg38UCSC Ensembl
chr6:168375581..168716980hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38341400
hg19341400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6516n223
Supporting Variantsnssv18216071
Samples
Known GenesDACT2, FRMD1, HGC6.3, KIF25, KIF25-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617771
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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