A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384091



Internal ID21041644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154679237..154686543hg38UCSC Ensembl
chr4:155600389..155607695hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg387307
hg197307
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212126
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384091
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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