A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607061



Internal ID20980132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144337205..144342334hg38UCSC Ensembl
chr6:144658341..144663470hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg385130
hg195130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140273
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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