A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414985



Internal ID21072538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40243529..40255910hg38UCSC Ensembl
chr6:40211268..40223649hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3812382
hg1912382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414985
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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