A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449795



Internal ID21107348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5940125..5941432hg38UCSC Ensembl
chr10:5982088..5983395hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381308
hg191308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982227
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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