A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442859



Internal ID21100412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16578019..16578468hg38UCSC Ensembl
chr10:16620018..16620467hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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