A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415224



Internal ID21072777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63387957..63392910hg38UCSC Ensembl
chr6:64097862..64102815hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg384954
hg194954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415224
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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