A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567263



Internal ID18421653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10479248..10530767hg38UCSC Ensembl
Outerchr6:10467735..10531767hg38UCSC Ensembl
Innerchr6:10479481..10531000hg19UCSC Ensembl
Outerchr6:10467968..10532000hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3864033
hg1964033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766010
Samples
Known GenesGCNT2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567263
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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