A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743683



Internal ID18717929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:74909247..74909416hg38UCSC Ensembl
Outerchr9:74909187..74909464hg38UCSC Ensembl
Innerchr9:77524163..77524332hg19UCSC Ensembl
Outerchr9:77524103..77524380hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3544936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743683
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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