A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892331



Internal ID19183151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37265836..37513971hg38UCSC Ensembl
Outerchr13:37244892..37589125hg38UCSC Ensembl
Innerchr13:37839973..38088108hg19UCSC Ensembl
Outerchr13:37819029..38163262hg19UCSC Ensembl
Innerchr13:36737973..36986108hg18UCSC Ensembl
Outerchr13:36717029..37061262hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38344234
hg19344234
hg18344234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791501, essv25788047, essv25788184, essv25787984
Samples
Known GenesLINC00547, POSTN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892331
Frequency
Sample Size3017
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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