A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673735



Internal ID9939840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28984737..28994053hg38UCSC Ensembl
chr7:29024353..29033669hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg389317
hg199317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6121061
SamplesNA19461
Known GenesLOC100506497
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673735
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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