A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035856



Internal ID20602896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44674401..44675800hg38UCSC Ensembl
chr17:42751769..42753168hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496962
Supporting Variants
Samples
Known GenesC17orf104
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035856
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00088


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