A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410177



Internal ID21067730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27235669..27351755hg38UCSC Ensembl
chr6:27203448..27319534hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38116087
hg19116087
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223643
Samples
Known GenesPOM121L2, PRSS16, VN1R10P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410177
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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