A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800230



Internal ID19169716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19357818..19371666hg38UCSC Ensembl
Innerchr7:19397441..19411289hg19UCSC Ensembl
Innerchr7:19363966..19377814hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3813849
hg1913849
hg1813849
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891084
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800230
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