A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6049080



Internal ID9825303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10858344..10863297hg38UCSC Ensembl
chr17:10761661..10766614hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg384954
hg194954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659921
Supporting Variants
SamplesNA20294
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6049080
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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