A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891109



Internal ID19185505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:51717993..51802005hg38UCSC Ensembl
Outerchr7:51717993..51802005hg38UCSC Ensembl
Innerchr7:51785689..51869701hg19UCSC Ensembl
Outerchr7:51785689..51869701hg19UCSC Ensembl
Innerchr7:51753183..51837195hg18UCSC Ensembl
Outerchr7:51753183..51837195hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3884013
hg1984013
hg1884013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780150
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891109
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