A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321008



Internal ID20854110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56065486..56075871hg38UCSC Ensembl
chr1:56531159..56541544hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3810386
hg1910386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202072
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321008
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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