A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381646



Internal ID21039199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:81327301..81328900hg38UCSC Ensembl
chr4:82248455..82250054hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381646
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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