A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953342



Internal ID17302216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:15034980..15103379hg38UCSC Ensembl
Outerchr21:16407301..16475700hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3868400
hg1968400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000656
SamplesBILGI_BIOE
Known GenesNRIP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953342
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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