A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893501



Internal ID19184321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:32596953..32621836hg38UCSC Ensembl
Outerchr1:32596953..32621836hg38UCSC Ensembl
Innerchr1:33062554..33087437hg19UCSC Ensembl
Outerchr1:33062554..33087437hg19UCSC Ensembl
Innerchr1:32835141..32860024hg18UCSC Ensembl
Outerchr1:32835141..32860024hg18UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3824884
hg1924884
hg1824884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783915
Samples
Known GenesZBTB8A, ZBTB8OS
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893501
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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