A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673696



Internal ID9939801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39839444..39845215hg38UCSC Ensembl
chr7:39879043..39884814hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385772
hg195772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6549624
SamplesNA19726
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673696
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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