A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5957079



Internal ID9029838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15365645..15368664hg38UCSC Ensembl
chr17:15268962..15271981hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg383020
hg193020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665781
Supporting Variants
SamplesHG00656
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5957079
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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