A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342107



Internal ID20999660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39831579..39866679hg38UCSC Ensembl
chr2:40058719..40093819hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3835101
hg1935101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342107
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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