A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316561



Internal ID20849641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100224748..100241773hg38UCSC Ensembl
chr1:100690304..100707329hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3817026
hg1917026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200289
Samples
Known GenesDBT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316561
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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