A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512929



Internal ID20886269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1175215..1185531hg38UCSC Ensembl
chr17:1078509..1088825hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3810317
hg1910317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191589
Samples
Known GenesABR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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