A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446455



Internal ID21104008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114695459..114738832hg38UCSC Ensembl
chr10:116455218..116498591hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3843374
hg1943374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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