A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744238



Internal ID18718484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128464682..128464861hg38UCSC Ensembl
Outerchr9:128464665..128464865hg38UCSC Ensembl
Innerchr9:131226961..131227140hg19UCSC Ensembl
Outerchr9:131226944..131227144hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545491
Supporting Variants
Samples
Known GenesODF2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744238
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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