A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv570e214



Internal ID22756464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35353236..35442365hg38UCSC Ensembl
chr17:33680255..33769384hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3889130
hg1989130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3640447, esv3640448, esv3640445
SamplesHG00351, HG00338, NA06989, HG00265, HG01269, HG00372
Known GenesSLFN11, SLFN12, SLFN13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv570e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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