A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414636



Internal ID21072189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54336301..54337100hg38UCSC Ensembl
chr6:54201099..54201898hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144738
Samples
Known GenesTINAG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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