A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355276



Internal ID21012829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:90282701..90306900hg38UCSC Ensembl
chr2:90467137..90491336hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3824200
hg1924200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355276
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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