A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640303



Internal ID7027078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27955805..27965833hg38UCSC Ensembl
Innerchr17:27955805..27965833hg38UCSC Ensembl
Outerchr17:27955305..27966333hg38UCSC Ensembl
chr17:26282831..26292859hg19UCSC Ensembl
Innerchr17:26282831..26292859hg19UCSC Ensembl
Outerchr17:26282331..26293359hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3810029
hg1910029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15655824
SamplesHG03052
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640303
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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