A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639469



Internal ID7026249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85771804..85776441hg38UCSC Ensembl
Innerchr16:85771854..85776391hg38UCSC Ensembl
Outerchr16:85771754..85776491hg38UCSC Ensembl
chr16:85805410..85810047hg19UCSC Ensembl
Innerchr16:85805460..85809997hg19UCSC Ensembl
Outerchr16:85805360..85810097hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg384638
hg194638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15552031
SamplesHG03849
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639469
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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