A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436038



Internal ID21093591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116781251..116783928hg38UCSC Ensembl
chr10:118540762..118543439hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg382678
hg192678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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