A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410116



Internal ID21067669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29434296..29435971hg38UCSC Ensembl
chr6:29402073..29403748hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381676
hg191676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141360
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410116
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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