A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455572



Internal ID21113125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117677346..117682306hg38UCSC Ensembl
chr10:119436857..119441817hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg384961
hg194961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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