A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038120



Internal ID20605160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78633955..78635365hg38UCSC Ensembl
chr17:76630037..76631447hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381411
hg191411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533452
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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