A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443358



Internal ID21100911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19010948..19046263hg38UCSC Ensembl
chr10:19299877..19335192hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3835316
hg1935316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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