A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640156



Internal ID7026931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18604097..18618729hg38UCSC Ensembl
chr17:18507410..18522042hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3814633
hg1914633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15641754, essv15641753, essv15641752
SamplesNA18986, HG04155, HG01396
Known GenesCCDC144B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640156
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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