A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950707



Internal ID17299581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:45182129..45204528hg38UCSC Ensembl
Outerchr1:45647801..45670200hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg3822400
hg1922400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997144
SamplesBILGI_BIOE
Known GenesZSWIM5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950707
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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