A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447303



Internal ID21104856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29072323..29074947hg38UCSC Ensembl
chr10:29361252..29363876hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg382625
hg192625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447303
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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