A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035072



Internal ID20602112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34821917..34829143hg38UCSC Ensembl
chr17:33148936..33156162hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387227
hg197227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506855
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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