A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438667



Internal ID21096220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121947897..121952937hg38UCSC Ensembl
chr10:123707412..123712452hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg385041
hg195041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978189
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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