A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891202



Internal ID19185598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:125622267..125769644hg38UCSC Ensembl
Outerchr7:125622267..125769644hg38UCSC Ensembl
Innerchr7:125262321..125409698hg19UCSC Ensembl
Outerchr7:125262321..125409698hg19UCSC Ensembl
Innerchr7:125049557..125196934hg18UCSC Ensembl
Outerchr7:125049557..125196934hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38147378
hg19147378
hg18147378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800063
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891202
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