A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437257



Internal ID21094810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12832980..12839760hg38UCSC Ensembl
chr10:12874980..12881760hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386781
hg196781
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186688
Samples
Known GenesLOC283070
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437257
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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