A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659108



Internal ID9925213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90789883..90800798hg38UCSC Ensembl
chr14:91256227..91267142hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3810916
hg1910916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6102765, essv5570072, essv5482460
SamplesNA11994, HG00116, HG01082
Known GenesTTC7B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659108
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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