A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317168



Internal ID20850252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:218897919..219046866hg38UCSC Ensembl
chr1:219071261..219220208hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38148948
hg19148948
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317168
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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