A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413937



Internal ID21071490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35617100..35628168hg38UCSC Ensembl
chr6:35584877..35595945hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3811069
hg1911069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227144
Samples
Known GenesFKBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413937
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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