A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892464



Internal ID19183284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19616004..19941099hg38UCSC Ensembl
Outerchr14:19245597..19955706hg38UCSC Ensembl
Innerchr14:20084006..20409258hg19UCSC Ensembl
Outerchr14:19833306..20423865hg19UCSC Ensembl
Innerchr14:19154003..19479098hg18UCSC Ensembl
Outerchr14:18903306..19493705hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38710110
hg19590560
hg18590400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791144, essv25791375
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEM
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892464
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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