A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437971



Internal ID21095524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68992104..68994983hg38UCSC Ensembl
chr10:70751860..70754739hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382880
hg192880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187732
Samples
Known GenesKIAA1279
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437971
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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