A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348951



Internal ID21006504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160176657..160177411hg38UCSC Ensembl
chr2:161033168..161033922hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205617
Samples
Known GenesITGB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348951
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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