A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546529



Internal ID18400919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:77041158..77041462hg38UCSC Ensembl
Outerchr10:77041086..77041496hg38UCSC Ensembl
Innerchr10:78800916..78801220hg19UCSC Ensembl
Outerchr10:78800844..78801254hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745276
Samples
Known GenesKCNMA1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546529
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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