A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6104966



Internal ID9383902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1696103..1704956hg38UCSC Ensembl
Outerchr19:1695944..1705135hg38UCSC Ensembl
Innerchr19:1696102..1704955hg19UCSC Ensembl
Outerchr19:1695943..1705134hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg389192
hg199192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665227
Supporting Variants
SamplesNA18576
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6104966
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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