A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612169



Internal ID20985240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101920658..102373813hg38UCSC Ensembl
chr6:102368533..102821688hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38453156
hg19453156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216491
Samples
Known GenesGRIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612169
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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