A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035085



Internal ID20602125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35068901..35070000hg38UCSC Ensembl
chr17:33395920..33397019hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502871
Supporting Variants
Samples
Known GenesRAD51L3-RFFL, RFFL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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