A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640102



Internal ID6680192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16455863..16524055hg38UCSC Ensembl
chr17:16359177..16427369hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3868193
hg1968193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15629812
SamplesNA19670
Known GenesFAM211A, FAM211A-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640102
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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