A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641251



Internal ID6681336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74886475..74890216hg38UCSC Ensembl
Innerchr17:74886525..74890167hg38UCSC Ensembl
Outerchr17:74886425..74890266hg38UCSC Ensembl
chr17:72882606..72886341hg19UCSC Ensembl
Innerchr17:72882656..72886292hg19UCSC Ensembl
Outerchr17:72882557..72886391hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg383742
hg193736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15740488
SamplesHG00693
Known GenesFADS6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641251
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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