A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6283465



Internal ID9260868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:63788181..63788550hg38UCSC Ensembl
Outerchr17:63788144..63788600hg38UCSC Ensembl
Innerchr17:61865541..61865910hg19UCSC Ensembl
Outerchr17:61865504..61865960hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658528
Supporting Variants
SamplesNA18516
Known GenesDDX42
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6283465
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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