A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664897



Internal ID9931002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3479058..3482687hg38UCSC Ensembl
Outerchr18:3479021..3482737hg38UCSC Ensembl
Innerchr18:3479056..3482685hg19UCSC Ensembl
Outerchr18:3479019..3482735hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383717
hg193717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6150734, essv6009540, essv6186337
SamplesNA19914, NA19374, NA19403
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664897
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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