A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532713



Internal ID20906074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48773800..48777506hg38UCSC Ensembl
chr17:46851162..46854868hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg383707
hg193707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187076
Samples
Known GenesTTLL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532713
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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