A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336311



Internal ID20993864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:227582101..227592200hg38UCSC Ensembl
chr2:228446817..228456916hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3810100
hg1910100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4300n223
Supporting Variantsnssv18206146
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336311
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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