A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659069



Internal ID9578488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28431369..28436625hg38UCSC Ensembl
chr7:28470988..28476244hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg385257
hg195257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5434754
SamplesHG00737
Known GenesCREB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659069
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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