A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641192



Internal ID7027966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72302777..72303736hg38UCSC Ensembl
Innerchr17:72302786..72303728hg38UCSC Ensembl
Outerchr17:72302769..72303745hg38UCSC Ensembl
chr17:70298918..70299877hg19UCSC Ensembl
Innerchr17:70298927..70299869hg19UCSC Ensembl
Outerchr17:70298910..70299886hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv586e214
Supporting Variantsessv15734912, essv15734911
SamplesNA20869, NA19214
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641192
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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