A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950339



Internal ID16952526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:26121910..26127709hg38UCSC Ensembl
Outerchr1:26448401..26454200hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997103
SamplesBILGI_BIOE
Known GenesPDIK1L
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950339
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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