A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354903



Internal ID21012456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:91426401..91470500hg38UCSC Ensembl
chr2:90397469..90441042hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3844100
hg1943574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4051n223
Supporting Variantsnssv18210682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354903
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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