A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669979



Internal ID9589398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19801698..19802075hg38UCSC Ensembl
Outerchr19:19801661..19802125hg38UCSC Ensembl
Innerchr19:19912507..19912884hg19UCSC Ensembl
Outerchr19:19912470..19912934hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5459342, essv6443773, essv5427105, essv6455087, essv6260543, essv6338418
SamplesNA18486, NA19403, NA19311, NA20348, NA19213, NA18505
Known GenesZNF506
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669979
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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