A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455146



Internal ID21112699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74906561..74926844hg38UCSC Ensembl
chr10:76666319..76686602hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3820284
hg1920284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984027
Samples
Known GenesKAT6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455146
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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