A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674401



Internal ID9940506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9754232..9757351hg38UCSC Ensembl
Outerchr17:9754181..9757413hg38UCSC Ensembl
Innerchr17:9657549..9660668hg19UCSC Ensembl
Outerchr17:9657498..9660730hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg383233
hg193233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6051152
SamplesNA19452
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674401
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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