A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2945866



Internal ID10965532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:864137..864137hg38UCSC Ensembl
chr17:767377..767377hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7215433
SamplesHuRef
Known GenesNXN
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2945866
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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