A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639985



Internal ID7026763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13185670..13207607hg38UCSC Ensembl
chr17:13088987..13110924hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3821938
hg1921938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15614702
SamplesHG00656
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639985
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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