A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037788



Internal ID20604828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64461504..64462881hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527290
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037788
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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