A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401241



Internal ID21058794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10726981..10752017hg38UCSC Ensembl
chr6:10727214..10752250hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3825037
hg1925037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216774
Samples
Known GenesTMEM14B, TMEM14C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401241
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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