A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950665



Internal ID16952852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:40031829..40062428hg38UCSC Ensembl
Outerchr1:40497501..40528100hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3830600
hg1930600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997130
SamplesBILGI_BIOE
Known GenesCAP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950665
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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