A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892785



Internal ID18836919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8364973..8565207hg38UCSC Ensembl
Outerchr16:8364973..8565207hg38UCSC Ensembl
Innerchr16:8414975..8615209hg19UCSC Ensembl
Outerchr16:8414975..8615209hg19UCSC Ensembl
Innerchr16:8354976..8555210hg18UCSC Ensembl
Outerchr16:8354976..8555210hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38200235
hg19200235
hg18200235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785255
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892785
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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