A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890777



Internal ID19185079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181028372..181068340hg38UCSC Ensembl
Outerchr5:181028372..181075321hg38UCSC Ensembl
Innerchr5:180455372..180495340hg19UCSC Ensembl
Outerchr5:180455372..180502321hg19UCSC Ensembl
Innerchr5:180387978..180427946hg18UCSC Ensembl
Outerchr5:180387978..180434927hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3846950
hg1946950
hg1846950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788294, essv25789384
Samples
Known GenesBTNL9, MIR8089
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890777
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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