A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891939



Internal ID18839649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:19507092..19565555hg38UCSC Ensembl
Outerchr11:19507092..19565555hg38UCSC Ensembl
Innerchr11:19528639..19587102hg19UCSC Ensembl
Outerchr11:19528639..19587102hg19UCSC Ensembl
Innerchr11:19485215..19543678hg18UCSC Ensembl
Outerchr11:19485215..19543678hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3858464
hg1958464
hg1858464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790308
Samples
Known GenesNAV2, NAV2-AS4, NAV2-AS5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891939
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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