A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037704



Internal ID20604744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76822810..76842900hg38UCSC Ensembl
chr17:74818892..74838982hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3820091
hg1920091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534529
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037704
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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