A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400644



Internal ID21058197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11486274..11486908hg38UCSC Ensembl
chr6:11486507..11487141hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400644
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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