A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790932



Internal ID19167279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62512881..63170073hg38UCSC Ensembl
Innerchr7:61973259..62630451hg19UCSC Ensembl
Innerchr7:61610694..62267886hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38657193
hg19657193
hg18657193
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891122
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=79
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790932
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