A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747760



Internal ID21392862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157278889..157282204hg38UCSC Ensembl
chr6:157699921..157703236hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383316
hg193316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434793
Supporting Variants
SamplesSMI041
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747760
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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