A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384022



Internal ID21041575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7756243..7858045hg38UCSC Ensembl
chr5:7756356..7858158hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38101803
hg19101803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216623
Samples
Known GenesADCY2, C5orf49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384022
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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