A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346527



Internal ID21004080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:83555376..83848189hg38UCSC Ensembl
chr2:83782500..84075313hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38292814
hg19292814
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3948n223
Supporting Variantsnssv18206426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346527
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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