A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216774



Internal ID20783814
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 StatusS
Merged Variantsnsv6401241
Supporting Variants
Samples
Known GenesTMEM14B, TMEM14C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216774
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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