A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641366



Internal ID7028140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80181760..80195698hg38UCSC Ensembl
chr17:78155559..78169497hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3813939
hg1913939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15756250, essv15756251
SamplesHG00634, HG00629
Known GenesCARD14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641366
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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