A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397371



Internal ID21054924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17945237..17949878hg38UCSC Ensembl
chr6:17945468..17950109hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384642
hg194642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143291
Samples
Known GenesKIF13A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397371
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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