A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6494616



Internal ID9472019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74051027..74052428hg38UCSC Ensembl
chr14:74517730..74519131hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664799
Supporting Variants
SamplesHG00231
Known GenesCCDC176
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6494616
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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