A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600515



Internal ID20973586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134638016..134640857hg38UCSC Ensembl
chr6:134959154..134961995hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg382842
hg192842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139443
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600515
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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