A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330573



Internal ID20863730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:216598601..216604100hg38UCSC Ensembl
chr1:216771943..216777442hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200577
Samples
Known GenesESRRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330573
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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