A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519097



Internal ID20892458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:54918041..54918659hg38UCSC Ensembl
chr17:52995402..52996020hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036881
Samples
Known GenesTOM1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519097
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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