A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752837



Internal ID18380397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:7661297..7662870hg38UCSC Ensembl
Outerchr17:7661097..7662927hg38UCSC Ensembl
Innerchr17:7564615..7566188hg19UCSC Ensembl
Outerchr17:7564415..7566245hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381831
hg191831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3554090
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752837
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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