A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544832



Internal ID18745908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38076703..38076802hg38UCSC Ensembl
chr9:38076700..38076799hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743579
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544832
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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