A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545642



Internal ID18400032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136672585..136673269hg38UCSC Ensembl
Outerchr9:136672575..136673284hg38UCSC Ensembl
Innerchr9:139567037..139567721hg19UCSC Ensembl
Outerchr9:139567027..139567736hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744389
Samples
Known GenesAGPAT2, EGFL7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545642
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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