A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893043



Internal ID18837177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73018638..73060921hg38UCSC Ensembl
Outerchr17:73018638..73060921hg38UCSC Ensembl
Innerchr17:71014777..71057060hg19UCSC Ensembl
Outerchr17:71014777..71057060hg19UCSC Ensembl
Innerchr17:68526372..68568655hg18UCSC Ensembl
Outerchr17:68526372..68568655hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3842284
hg1942284
hg1842284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786022
Samples
Known GenesSLC39A11
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893043
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer