A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744676



Internal ID18718922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13487503..13488510hg38UCSC Ensembl
Outerchr10:13487488..13488601hg38UCSC Ensembl
Innerchr10:13529503..13530510hg19UCSC Ensembl
Outerchr10:13529488..13530601hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381114
hg191114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545929
Supporting Variants
Samples
Known GenesBEND7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744676
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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