A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952134



Internal ID17301008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:228000700..228021699hg38UCSC Ensembl
Outerchr1:228188401..228209400hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3821000
hg1921000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000305
SamplesBILGI_BIOE
Known GenesWNT3A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952134
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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