A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447611



Internal ID21105164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44460500..44465296hg38UCSC Ensembl
chr10:44955948..44960744hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg384797
hg194797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447611
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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