A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6151042



Internal ID9889563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47767733..47774924hg38UCSC Ensembl
chr19:48270990..48278181hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg387192
hg197192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665970
Supporting Variants
SamplesNA20769
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6151042
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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