A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892525



Internal ID18836659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16913478..16955930hg38UCSC Ensembl
Outerchr1:16913478..16955930hg38UCSC Ensembl
Innerchr1:17239973..17282425hg19UCSC Ensembl
Outerchr1:17239973..17282425hg19UCSC Ensembl
Innerchr1:17112560..17155012hg18UCSC Ensembl
Outerchr1:17112560..17155012hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3842453
hg1942453
hg1842453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783921
Samples
Known GenesCROCC
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892525
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