A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893849



Internal ID19184669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:193418687..193434805hg38UCSC Ensembl
Outerchr3:193418687..193434805hg38UCSC Ensembl
Innerchr3:193136476..193152594hg19UCSC Ensembl
Outerchr3:193136476..193152594hg19UCSC Ensembl
Innerchr3:194619170..194635288hg18UCSC Ensembl
Outerchr3:194619170..194635288hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3816119
hg1916119
hg1816119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786181, essv25798602
Samples
Known GenesATP13A4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893849
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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