A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400096



Internal ID21057649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23218901..23229800hg38UCSC Ensembl
chr6:23219129..23230028hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3810900
hg1910900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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