A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641314



Internal ID6681399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77415181..77416957hg38UCSC Ensembl
Innerchr17:77415207..77416932hg38UCSC Ensembl
Outerchr17:77415156..77416983hg38UCSC Ensembl
chr17:75411263..75413039hg19UCSC Ensembl
Innerchr17:75411289..75413014hg19UCSC Ensembl
Outerchr17:75411238..75413065hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381777
hg191777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15748450
SamplesHG04093
Known GenesSEPT9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641314
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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