A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380079



Internal ID21037632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7380314..7595214hg38UCSC Ensembl
chr5:7380427..7595327hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38214901
hg19214901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216334
Samples
Known GenesADCY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380079
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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