A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662904



Internal ID9929009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19515845..19516508hg38UCSC Ensembl
chr17:19419158..19419821hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6282244, essv5790977, essv6286132
SamplesHG01060, NA19130, NA19257
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662904
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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