A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396343



Internal ID21053896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75630073..76081031hg38UCSC Ensembl
chr6:76339789..76790748hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38450959
hg19450960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229010
Samples
Known GenesIMPG1, MYO6, SENP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396343
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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