A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv19n73



Internal ID22782625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4247865..4249508hg38UCSC Ensembl
chr10:4290057..4291700hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381644
hg191644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv955595, nsv951240
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)dgv19n73
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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