A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038614



Internal ID20605654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79631645..79634046hg38UCSC Ensembl
chr17_gl000204_random:77582..79983hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382402
hg192402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517845
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038614
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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