A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443290



Internal ID21100843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49346065..49356190hg38UCSC Ensembl
chr10:50554110..50564235hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3810126
hg1910126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980019
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443290
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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