A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397877



Internal ID21055430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68738434..68738834hg38UCSC Ensembl
chr6:69448326..69448726hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143843
Samples
Known GenesBAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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