A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640409



Internal ID7027184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33572945..33576610hg38UCSC Ensembl
Innerchr17:33572945..33576610hg38UCSC Ensembl
Outerchr17:33572717..33576852hg38UCSC Ensembl
chr17:31899964..31903629hg19UCSC Ensembl
Innerchr17:31899964..31903629hg19UCSC Ensembl
Outerchr17:31899736..31903871hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383666
hg193666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15661280, essv15661281
SamplesHG01985, NA19143
Known GenesASIC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640409
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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