A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953995



Internal ID17302869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:234774354..234800253hg38UCSC Ensembl
Outerchr1:234910101..234936000hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3825900
hg1925900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001624
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953995
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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