A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435663



Internal ID21093216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127752089..127804276hg38UCSC Ensembl
chr10:129550353..129602540hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3852188
hg1952188
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435663
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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