A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546724



Internal ID18401114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97275119..97277636hg38UCSC Ensembl
Outerchr10:97274995..97277673hg38UCSC Ensembl
Innerchr10:99034876..99037393hg19UCSC Ensembl
Outerchr10:99034752..99037430hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382679
hg192679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745471
Samples
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546724
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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