A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602852



Internal ID20975923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168128177..168614708hg38UCSC Ensembl
chr6:168528857..169015388hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38486532
hg19486532
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216104
Samples
Known GenesDACT2, SMOC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602852
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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