A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951573



Internal ID16953760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46628717..46644016hg38UCSC Ensembl
Outerchr10:46905601..46920900hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3815300
hg1915300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997964
SamplesBILGI_BIOE
Known GenesFAM35BP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951573
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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