A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640445



Internal ID7027220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35353236..35434799hg38UCSC Ensembl
chr17:33680255..33761818hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3881564
hg1981564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv570e214
Supporting Variantsessv15664513, essv15664512, essv15664510, essv15664511
SamplesHG00351, HG00338, NA06989, HG01269
Known GenesSLFN11, SLFN12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640445
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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