A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640404



Internal ID7027179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33436827..33443746hg38UCSC Ensembl
Innerchr17:33437327..33443246hg38UCSC Ensembl
Outerchr17:33435827..33444746hg38UCSC Ensembl
chr17:31763845..31770764hg19UCSC Ensembl
Innerchr17:31764345..31770264hg19UCSC Ensembl
Outerchr17:31762845..31771764hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg386920
hg196920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15661263
SamplesNA18577
Known GenesASIC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640404
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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