A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327902



Internal ID20861046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:82439365..82539739hg38UCSC Ensembl
chr1:82905048..83005422hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38100375
hg19100375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327902
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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