A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556028



Internal ID18410418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11184253..11185686hg38UCSC Ensembl
Outerchr19:11184040..11185898hg38UCSC Ensembl
Innerchr19:11294929..11296362hg19UCSC Ensembl
Outerchr19:11294716..11296574hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381859
hg191859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754775
Samples
Known GenesKANK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556028
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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