A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614157



Internal ID20987228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100953141..100984846hg38UCSC Ensembl
chr6:101401017..101432722hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3831706
hg1931706
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614157
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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