A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5953711



Internal ID8931114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77487590..77487834hg38UCSC Ensembl
Outerchr17:77487463..77487960hg38UCSC Ensembl
Innerchr17:75483916..75483672hg19UCSC Ensembl
Outerchr17:75483545..75484042hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672897
Supporting Variants
SamplesNA19372
Known GenesSEPT9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5953711
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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