A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640448



Internal ID7027223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35353788..35442365hg38UCSC Ensembl
chr17:33680807..33769384hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3888578
hg1988578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv570e214
Supporting Variantsessv15664521, essv15664522
SamplesNA06989, HG01269
Known GenesSLFN11, SLFN12, SLFN13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640448
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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