A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5580868



Internal ID8961844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:874621..874730hg38UCSC Ensembl
Outerchr17:874584..874780hg38UCSC Ensembl
Innerchr17:777861..777970hg19UCSC Ensembl
Outerchr17:777824..778020hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666176
Supporting Variants
SamplesHG00531
Known GenesNXN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5580868
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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