A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977494



Internal ID20544534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116245803..116250083hg38UCSC Ensembl
chr10:118005315..118009595hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg384281
hg194281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440078
Supporting Variants
Samples
Known GenesGFRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977494
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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