A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397771



Internal ID21055324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28025839..28034494hg38UCSC Ensembl
chr6:27993617..28002272hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg388656
hg198656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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