A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892422



Internal ID19183242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90973468..91070852hg38UCSC Ensembl
Outerchr13:90973468..91070852hg38UCSC Ensembl
Innerchr13:91625722..91723106hg19UCSC Ensembl
Outerchr13:91625722..91723106hg19UCSC Ensembl
Innerchr13:90423723..90521107hg18UCSC Ensembl
Outerchr13:90423723..90521107hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3897385
hg1997385
hg1897385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782533
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892422
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