A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605962



Internal ID20979033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154964405..154975970hg38UCSC Ensembl
chr6:155285539..155297104hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3811566
hg1911566
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605962
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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