A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6468059



Internal ID9453456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77175055..77176543hg38UCSC Ensembl
chr7:76804372..76805860hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381489
hg191489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667964
Supporting Variants
SamplesNA18873
Known GenesCCDC146
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6468059
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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