A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039039



Internal ID20606079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77797301..77802300hg38UCSC Ensembl
chr17:75793383..75798382hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530733
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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