A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353282



Internal ID21010835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:171912779..171920649hg38UCSC Ensembl
chr2:172769289..172777159hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg387871
hg197871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207410
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353282
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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