A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666894



Internal ID9932999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142312583..142344902hg38UCSC Ensembl
chr7:142012406..142044733hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3832320
hg1932328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1243e199
Supporting Variantsessv6360886, essv5865366, essv6432016
SamplesHG01051, HG00653, NA19449
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666894
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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