A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3356636



Internal ID15203616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:26963199..26984197hg38UCSC Ensembl
Innerchr17:26964199..26983197hg38UCSC Ensembl
Outerchr17:26962199..26985197hg38UCSC Ensembl
chr17:25290225..25311223hg19UCSC Ensembl
Innerchr17:25291225..25310223hg19UCSC Ensembl
Outerchr17:25289225..25312223hg19UCSC Ensembl
chr17:22314352..22335350hg18UCSC Ensembl
Innerchr17:22315352..22334350hg18UCSC Ensembl
Outerchr17:22313352..22336350hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3820999
hg1920999
hg1820999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1723e59
Supporting Variantsessv8690700
SamplesNA12891
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3356636
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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