A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5815764



Internal ID9804571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:65118532..65122455hg38UCSC Ensembl
Outerchr17:65118495..65122505hg38UCSC Ensembl
Innerchr17:63114650..63118573hg19UCSC Ensembl
Outerchr17:63114613..63118623hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg384011
hg194011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658875
Supporting Variants
SamplesNA19901
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5815764
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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