A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453738



Internal ID21111291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92472457..92473008hg38UCSC Ensembl
chr10:94232214..94232765hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985427
Samples
Known GenesIDE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453738
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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