A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444719



Internal ID21102272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30807032..30826373hg38UCSC Ensembl
chr10:31095961..31115302hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3819342
hg1919342
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444719
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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