A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663502



Internal ID9929607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10724655..10749292hg38UCSC Ensembl
chr6:10724888..10749525hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3824638
hg1924638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5817023
SamplesNA18986
Known GenesTMEM14B, TMEM14C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663502
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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