A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661899



Internal ID9928004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:924423..925435hg38UCSC Ensembl
Outerchr17:924266..925588hg38UCSC Ensembl
Innerchr17:827663..828675hg19UCSC Ensembl
Outerchr17:827506..828828hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381323
hg191323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6481756
SamplesHG00671
Known GenesNXN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661899
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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