A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499383



Internal ID20872602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4737312..4738041hg38UCSC Ensembl
chr17:4640607..4641336hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035974
Samples
Known GenesCXCL16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499383
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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