A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035962



Internal ID20603002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4712449..4714409hg38UCSC Ensembl
chr17:4615744..4617704hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg381961
hg191961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506963
Supporting Variants
Samples
Known GenesARRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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