A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447369



Internal ID21104922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29088121..29109693hg38UCSC Ensembl
chr10:29377050..29398622hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3821573
hg1921573
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195851
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447369
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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