A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407600



Internal ID21065153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43809713..43811264hg38UCSC Ensembl
chr6:43777450..43779001hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381552
hg191552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407600
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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