A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338971



Internal ID20996524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168652501..168662300hg38UCSC Ensembl
chr2:169509011..169518810hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg389800
hg199800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207377
Samples
Known GenesCERS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338971
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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