A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451736



Internal ID21109289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:108996264..109095835hg38UCSC Ensembl
chr10:110756022..110855593hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3899572
hg1999572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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