A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611927



Internal ID20984998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149621377..149628362hg38UCSC Ensembl
chr6:149942513..149949498hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg386986
hg196986
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217091
Samples
Known GenesKATNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611927
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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