A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15739027



Internal ID5894873
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641245
Supporting Variants
SamplesNA19315
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15739027
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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