A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9755023



Internal ID18382583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:30526449..30526703hg38UCSC Ensembl
Outerchr19:30526383..30526791hg38UCSC Ensembl
Innerchr19:31017356..31017610hg19UCSC Ensembl
Outerchr19:31017290..31017698hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3556276
Supporting Variants
Samples
Known GenesZNF536
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9755023
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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