A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954826



Internal ID16957013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:207134677..207164376hg38UCSC Ensembl
Outerchr2:207999401..208029100hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3829700
hg1929700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003109
SamplesBILGI_BIOE
Known GenesKLF7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954826
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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