A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521425



Internal ID20894786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49254937..49260118hg38UCSC Ensembl
chr17:47332299..47337480hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg385182
hg195182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036117
Samples
Known GenesFLJ40194
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521425
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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