A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519084



Internal ID20892445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50350142..50350526hg38UCSC Ensembl
chr17:48427503..48427887hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036163
Samples
Known GenesXYLT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519084
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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