A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400434



Internal ID21057987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53618843..53619584hg38UCSC Ensembl
chr6:53483641..53484382hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144680
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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