A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952226



Internal ID17301100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:161539911..161567010hg38UCSC Ensembl
Outerchr1:161509701..161536800hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3827100
hg1927100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998323
SamplesBILGI_BIOE
Known GenesFCGR3A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952226
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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