A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517112



Internal ID20890473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78788228..78791198hg38UCSC Ensembl
chr17:76784310..76787280hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382971
hg192971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517112
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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