A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546732



Internal ID18401122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97956522..97956677hg38UCSC Ensembl
Outerchr10:97956513..97956687hg38UCSC Ensembl
Innerchr10:99716279..99716434hg19UCSC Ensembl
Outerchr10:99716270..99716444hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745479
Samples
Known GenesCRTAC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546732
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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