A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780172



Internal ID19165425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45749458..45775632hg38UCSC Ensembl
Innerchr11:45771009..45797183hg19UCSC Ensembl
Innerchr11:45727585..45753759hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3826175
hg1926175
hg1826175
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891976
Supporting Variants
Samples
Known GenesDKFZp779M0652
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780172
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