A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425738



Internal ID21083291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2898201..2908258hg38UCSC Ensembl
chr9:2898201..2908258hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3810058
hg1910058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425738
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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