A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641109



Internal ID7027883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68218865..68234933hg38UCSC Ensembl
Innerchr17:68219365..68234433hg38UCSC Ensembl
Outerchr17:68217865..68235933hg38UCSC Ensembl
chr17:66215006..66231074hg19UCSC Ensembl
Innerchr17:66215506..66230574hg19UCSC Ensembl
Outerchr17:66214006..66232074hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3816069
hg1916069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15730492
SamplesHG01341
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641109
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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