A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434793



Internal ID21396795
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 StatusM
Merged Variantsdgv722n172
Supporting Variantsnssv15747760, nssv15750935, nssv15754485, nssv15747912, nssv15747084
SamplesBTQ038, BTQ055, MDQ010, SMI041, SMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434793
Frequency
Sample Size15
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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