A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5660487



Internal ID8637890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28534721..28535564hg38UCSC Ensembl
chr7:28574339..28575182hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg38844
hg19844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659026
Supporting Variants
SamplesHG01149
Known GenesCREB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5660487
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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