A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893947



Internal ID19184801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68631558..68691052hg38UCSC Ensembl
Outerchr4:68631558..68709989hg38UCSC Ensembl
Innerchr4:69497276..69556770hg19UCSC Ensembl
Outerchr4:69497276..69575707hg19UCSC Ensembl
Innerchr4:69179871..69239365hg18UCSC Ensembl
Outerchr4:69179871..69258302hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3878432
hg1978432
hg1878432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800882, essv25780984
Samples
Known GenesUGT2B15
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893947
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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