A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038061



Internal ID20605101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72042938..72043652hg38UCSC Ensembl
chr17:70039079..70039793hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524830
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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