A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413791



Internal ID21071344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79236101..79238800hg38UCSC Ensembl
chr5:78531924..78534623hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214183
Samples
Known GenesJMY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413791
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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