A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953231



Internal ID16955418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:87227951..87252550hg38UCSC Ensembl
Outerchr3:87277101..87301700hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg3824600
hg1924600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001428
SamplesBILGI_BIOE
Known GenesCHMP2B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953231
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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