A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5968683



Internal ID9504392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41398630..41403447hg38UCSC Ensembl
chr7:41438228..41443045hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg384818
hg194818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666905
Supporting Variants
SamplesNA18984
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5968683
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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