A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377332



Internal ID21034885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44359144..44361313hg38UCSC Ensembl
chr5:44359246..44361415hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg382170
hg192170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214129
Samples
Known GenesFGF10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377332
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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