A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511858



Internal ID20885188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35353401..35441700hg38UCSC Ensembl
chr17:33680420..33768719hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3888300
hg1988300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3086n223
Supporting Variantsnssv18035100
Samples
Known GenesSLFN11, SLFN12, SLFN13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511858
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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