A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502735



Internal ID20875983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28889672..28890894hg38UCSC Ensembl
chr17:27216690..27217912hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381223
hg191223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035216
Samples
Known GenesFLOT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502735
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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