A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639824



Internal ID7026602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5869326..5888585hg38UCSC Ensembl
chr17:5772646..5791905hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3819260
hg1919260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv558e214
Supporting Variantsessv15601063
SamplesHG03919
Known GenesLOC339166
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639824
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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