A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665948



Internal ID9932053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67752503..67758011hg38UCSC Ensembl
chr7:67217490..67222998hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg385509
hg195509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6415827, essv6187167
SamplesNA19376, NA19430
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665948
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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