A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520500



Internal ID20893861
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 StatusM
Merged Variants
Supporting Variantsnssv18188589
Samples
Known GenesANKFN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520500
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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