A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507429



Internal ID20880720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4267032..4306754hg38UCSC Ensembl
chr17:4170327..4210049hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3839723
hg1939723
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182862
Samples
Known GenesUBE2G1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507429
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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