A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316585



Internal ID20849665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84904175..84915388hg38UCSC Ensembl
chr1:85369858..85381071hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3811214
hg1911214
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316585
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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