A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892828



Internal ID19183648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31568951..31618828hg38UCSC Ensembl
Outerchr16:31566892..31623178hg38UCSC Ensembl
Innerchr16:31580272..31630149hg19UCSC Ensembl
Outerchr16:31578213..31634499hg19UCSC Ensembl
Innerchr16:31487773..31537650hg18UCSC Ensembl
Outerchr16:31485714..31542000hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3856287
hg1956287
hg1856287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788899, essv25789213, essv25792660, essv25788895, essv25788561
Samples
Known GenesYBX3P1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892828
Frequency
Sample Size3017
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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