A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661151



Internal ID9927256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9300131..9302958hg38UCSC Ensembl
Outerchr17:9299974..9303111hg38UCSC Ensembl
Innerchr17:9203448..9206275hg19UCSC Ensembl
Outerchr17:9203291..9206428hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg383138
hg193138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6523034
SamplesHG00335
Known GenesSTX8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661151
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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