A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745277



Internal ID18372837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77376558..77376641hg38UCSC Ensembl
chr10:79136316..79136399hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546530
Supporting Variants
Samples
Known GenesKCNMA1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745277
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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