A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355782



Internal ID21013335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20002895..20004510hg38UCSC Ensembl
chr4:20004518..20006133hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg381616
hg191616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355782
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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