A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660504



Internal ID9926609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104189592..104189736hg38UCSC Ensembl
Outerchr14:104189553..104189793hg38UCSC Ensembl
Innerchr14:104655929..104656073hg19UCSC Ensembl
Outerchr14:104655890..104656130hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6405520, essv6203568, essv6303360, essv5861453, essv6512294, essv5644059, essv6260540, essv5625935, essv5910901, essv6519606, essv6500401, essv6218444, essv6246071, essv6325359, essv6023422, essv5834533, essv6178466, essv6583107, essv5702888, essv5988077, essv5454110, essv6517833, essv5625619, essv6159241, essv5989522, essv6577420, essv6205404, essv6480063, essv6095151
SamplesNA19700, HG00608, NA11829, NA18486, NA19920, NA18988, NA19916, NA19172, NA18520, NA18908, NA19247, NA20525, HG00157, NA19059, NA18963, NA19012, NA19652, NA19834, NA19835, NA20792, NA19248, NA19472, NA19716, NA18873, NA19780, NA19213, NA19900, NA18984, NA18488
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660504
Frequency
Sample Size1151
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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