A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640064



Internal ID7026842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15209141..15256214hg38UCSC Ensembl
chr17:15112458..15159531hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3847074
hg1947074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15624268
SamplesHG03572
Known GenesMIR4731, PMP22
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640064
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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