A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344041



Internal ID21001594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234651418..234653445hg38UCSC Ensembl
chr2:235560062..235562089hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg382028
hg192028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208329
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344041
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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