A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977648



Internal ID20544688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107516406..107516984hg38UCSC Ensembl
chr10:109276164..109276742hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449165
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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