A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445229



Internal ID21102782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4827318..4827502hg38UCSC Ensembl
chr10:4869510..4869694hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979974
Samples
Known GenesAKR1E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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