A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954902



Internal ID16957089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:21599708..21654507hg38UCSC Ensembl
Outerchr1:21926201..21981000hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3854800
hg1954800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003151
SamplesBILGI_BIOE
Known GenesRAP1GAP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954902
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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