A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500660



Internal ID20873888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39760467..39761812hg38UCSC Ensembl
chr17:37916720..37918065hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381346
hg191346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179393
Samples
Known GenesIKZF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500660
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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