A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604553



Internal ID20977624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106901570..106908382hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604553
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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