A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372677



Internal ID21030230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14733101..14735015hg38UCSC Ensembl
chr4:14734725..14736639hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg381915
hg191915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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