A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340069



Internal ID20997622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214231601..214243500hg38UCSC Ensembl
chr2:215096325..215108224hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3811900
hg1911900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208163
Samples
Known GenesSPAG16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340069
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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