A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505771



Internal ID20879044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77397304..77431471hg38UCSC Ensembl
chr15:77689646..77723813hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3834168
hg1934168
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179955
Samples
Known GenesHMG20A, PEAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505771
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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