A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336553



Internal ID20994106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206797601..206805300hg38UCSC Ensembl
chr2:207662325..207670024hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4268n223
Supporting Variantsnssv18208104
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336553
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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