A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426344



Internal ID21083897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7194944..7205486hg38UCSC Ensembl
chr9:7194944..7205486hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3810543
hg1910543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227912
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426344
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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