A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317428



Internal ID20850513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:188752949..189325996hg38UCSC Ensembl
chr1:188722080..189295126hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38573048
hg19573047
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv467n223
Supporting Variantsnssv18199155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317428
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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