A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521077



Internal ID20894438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62199557..62227904hg38UCSC Ensembl
chr17:60276918..60305265hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3828348
hg1928348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521077
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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