A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525877



Internal ID20899238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81477998..81555207hg38UCSC Ensembl
chr17:79445024..79522233hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3877210
hg1977210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192200
Samples
Known GenesACTG1, C17orf70, FSCN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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