A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613438



Internal ID20986509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146734804..146740288hg38UCSC Ensembl
chr6:147055940..147061424hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg385485
hg195485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139076
Samples
Known GenesADGB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613438
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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