A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352129



Internal ID21009682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200484382..200485555hg38UCSC Ensembl
chr2:201349105..201350278hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381174
hg191174
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352129
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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