A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521600



Internal ID20894961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53639912..53968347hg38UCSC Ensembl
chr17:51717273..52045708hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38328436
hg19328436
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186684
Samples
Known GenesKIF2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521600
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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