A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952066



Internal ID16954253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:211259059..211260258hg38UCSC Ensembl
Outerchr1:211432401..211433600hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000185
SamplesBILGI_BIOE
Known GenesRCOR3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952066
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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