A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455104



Internal ID21112657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121450083..121450640hg38UCSC Ensembl
chr10:123209597..123210154hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980552
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455104
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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