A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891083



Internal ID19185479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18895687..18908332hg38UCSC Ensembl
Outerchr7:18895687..18908332hg38UCSC Ensembl
Innerchr7:18935310..18947955hg19UCSC Ensembl
Outerchr7:18935310..18947955hg19UCSC Ensembl
Innerchr7:18901835..18914480hg18UCSC Ensembl
Outerchr7:18901835..18914480hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3812646
hg1912646
hg1812646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788632
Samples
Known GenesHDAC9
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891083
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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