A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667655



Internal ID9587074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:17934061..17934311hg38UCSC Ensembl
Outerchr19:17934024..17934361hg38UCSC Ensembl
Innerchr19:18044870..18045120hg19UCSC Ensembl
Outerchr19:18044833..18045170hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5615004, essv6293599, essv6450628, essv6570192
SamplesNA18519, NA19917, NA18871, NA19257
Known GenesCCDC124
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667655
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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