A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035102



Internal ID20602142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35353601..35440400hg38UCSC Ensembl
chr17:33680620..33767419hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3886800
hg1986800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510522
Supporting Variants
Samples
Known GenesSLFN11, SLFN12, SLFN13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035102
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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