A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657778



Internal ID9923883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35627672..35628077hg38UCSC Ensembl
chr19:36118574..36118979hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5706067, essv5722855, essv5525818, essv5996529, essv5925450, essv6095459, essv6163134, essv6527512, essv5819894, essv6554972, essv5673916, essv6026205, essv6082463, essv5704542, essv5943403, essv6204730, essv5731145, essv6249345, essv6243795, essv5401858, essv6428798, essv6065608
SamplesNA19703, NA18924, NA19332, NA18507, NA19198, NA19130, NA19404, NA18874, NA19985, HG01171, NA18933, NA19327, NA18907, NA20299, NA19469, NA19147, NA19331, HG01375, NA19334, NA19324, NA19360, HG00554
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657778
Frequency
Sample Size1151
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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