A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892297



Internal ID18836431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19837561..19935063hg38UCSC Ensembl
Outerchr13:19803308..20022425hg38UCSC Ensembl
Innerchr13:20411701..20509203hg19UCSC Ensembl
Outerchr13:20377448..20596565hg19UCSC Ensembl
Innerchr13:19309701..19407203hg18UCSC Ensembl
Outerchr13:19275448..19494565hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38219118
hg19219118
hg18219118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790458, essv25787803, essv25787770
Samples
Known GenesZMYM2, ZMYM5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892297
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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