A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641245



Internal ID7028019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74548318..74559640hg38UCSC Ensembl
Innerchr17:74548322..74559637hg38UCSC Ensembl
Outerchr17:74548315..74559644hg38UCSC Ensembl
chr17:72544457..72555779hg19UCSC Ensembl
Innerchr17:72544461..72555776hg19UCSC Ensembl
Outerchr17:72544454..72555783hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3811323
hg1911323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15739027, essv15739026
SamplesNA19315, NA19307
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641245
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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