A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893157



Internal ID18837291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2937669..2953811hg38UCSC Ensembl
Outerchr19:2937669..2953811hg38UCSC Ensembl
Innerchr19:2937667..2953809hg19UCSC Ensembl
Outerchr19:2937667..2953809hg19UCSC Ensembl
Innerchr19:2888667..2904809hg18UCSC Ensembl
Outerchr19:2888667..2904809hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3816143
hg1916143
hg1816143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782303, essv25801642
Samples
Known GenesZNF77
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893157
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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