A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778315



Internal ID19161445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34807021..34848540hg38UCSC Ensembl
Innerchr2:35032088..35073607hg19UCSC Ensembl
Innerchr2:34885592..34927111hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3841520
hg1941520
hg1841520
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891815
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778315
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