A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508814



Internal ID20882118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35050123..35052011hg38UCSC Ensembl
chr17:33377142..33379030hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381889
hg191889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035083
Samples
Known GenesRAD51L3-RFFL, RFFL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508814
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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