A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953962



Internal ID17302836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:233826455..233827954hg38UCSC Ensembl
Outerchr1:233962201..233963700hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001619
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953962
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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