A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703897



Internal ID21376173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108221234..108221307hg38UCSC Ensembl
chr6:108542438..108542511hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392585
Supporting Variants
Samples
Known GenesSNX3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703897
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00862069


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