A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396067



Internal ID21053620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34216505..34217838hg38UCSC Ensembl
chr6:34184282..34185615hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381334
hg191334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140874
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396067
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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