A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400396



Internal ID21057949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95600101..95606000hg38UCSC Ensembl
chr6:96047977..96053876hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235992
Samples
Known GenesMANEA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400396
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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