A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562600



Internal ID18763676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136302933..136307064hg38UCSC Ensembl
Outerchr3:136302087..136307407hg38UCSC Ensembl
Innerchr3:136021775..136025906hg19UCSC Ensembl
Outerchr3:136020929..136026249hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg385321
hg195321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv303e215
Supporting Variantsessv9761347
Samples
Known GenesPCCB
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562600
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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