A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499787



Internal ID20873011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4220701..4227100hg38UCSC Ensembl
chr17:4123996..4130395hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194827
Samples
Known GenesANKFY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499787
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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