A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188589



Internal ID20755629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56211488..56216975hg38UCSC Ensembl
chr17:54288849..54294336hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg385488
hg195488
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520500
Supporting Variants
Samples
Known GenesANKFN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188589
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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