A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449643



Internal ID21107196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13265797..13275810hg38UCSC Ensembl
chr10:13307797..13317810hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3810014
hg1910014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978562
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449643
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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