A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326331



Internal ID20859466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203108794..203113891hg38UCSC Ensembl
chr1:203077922..203083019hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg385098
hg195098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326331
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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