A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640900



Internal ID6680985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59009807..59014668hg38UCSC Ensembl
Innerchr17:59009807..59014668hg38UCSC Ensembl
Outerchr17:59009307..59015168hg38UCSC Ensembl
chr17:57087168..57092029hg19UCSC Ensembl
Innerchr17:57087168..57092029hg19UCSC Ensembl
Outerchr17:57086668..57092529hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg384862
hg194862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15711250, essv15711252, essv15711251
SamplesHG01064, HG01176, HG01303
Known GenesTRIM37
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640900
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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