A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035565



Internal ID20602605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51988401..52030600hg38UCSC Ensembl
chr17:50065761..50107960hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3842200
hg1942200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522200
Supporting Variants
Samples
Known GenesCA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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