A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892876



Internal ID19183696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65380246..65543462hg38UCSC Ensembl
Outerchr16:65363379..65688177hg38UCSC Ensembl
Innerchr16:65414149..65577365hg19UCSC Ensembl
Outerchr16:65397282..65722080hg19UCSC Ensembl
Innerchr16:63971650..64134866hg18UCSC Ensembl
Outerchr16:63954783..64279581hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38324799
hg19324799
hg18324799
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779975, essv25790861
Samples
Known GenesLINC00922
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892876
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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