A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437786



Internal ID21095339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:531300..607954hg38UCSC Ensembl
chr10:577240..653894hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3876655
hg1976655
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179248
Samples
Known GenesDIP2C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437786
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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