A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617518



Internal ID20990589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146170013..146176838hg38UCSC Ensembl
chr6:146491149..146497974hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg386826
hg196826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139015
Samples
Known GenesGRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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