A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441988



Internal ID21099541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70069149..70076885hg38UCSC Ensembl
chr10:71828905..71836641hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg387737
hg197737
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179107
Samples
Known GenesH2AFY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441988
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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