A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6082552



Internal ID9521269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:50818962..50820755hg38UCSC Ensembl
Outerchr17:50818925..50820805hg38UCSC Ensembl
Innerchr17:48896323..48898116hg19UCSC Ensembl
Outerchr17:48896286..48898166hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657946
Supporting Variants
SamplesNA19009
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6082552
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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