A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443407



Internal ID21100960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61215201..61217000hg38UCSC Ensembl
chr9:43603743..43605540hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381800
hg191798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222058
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443407
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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