A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5888113



Internal ID8865516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21651521..22709008hg38UCSC Ensembl
Outerchr17:21651521..22709043hg38UCSC Ensembl
Innerchr17:21550207..22208335hg19UCSC Ensembl
Outerchr17:21550173..22208370hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381057523
hg19658198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662973
Supporting Variants
SamplesHG00560
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5888113
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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