A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339201



Internal ID20996754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176377999..176395901hg38UCSC Ensembl
chr2:177242727..177260629hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3817903
hg1917903
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339201
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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